Production of multimeric proteins

ABSTRACT

The present invention provides a new, effective and efficient method of producing multimeric proteins in an individual. Multimeric proteins include associated multimeric proteins (two or more associated polypeptides) and multivalent multimeric proteins (a single polypeptide encoded by more than one gene of interest). Expression and/or formation of the multimeric protein in the individual is achieved by administering a polynucleotide cassette containing genes of interest that encode portions of the multimeric protein to the individual. The polynucleotide cassette may additionally contain one or more pro sequences, prepro sequences, cecropin prepro sequences, and/or cleavage site sequences.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] The present application is a continuation-in-part of U.S. patent application Ser. No. 10/609,019 filed on Jun. 26, 2003, and claims the priority benefit of U.S. Provisional Patent Application No. 60/441,392 filed Jan. 21, 2003; U.S. Provisional Patent Application No. 60/441,377 filed Jan. 21, 2003; U.S. Provisional Patent Application No. 60/441,502 filed Jan. 21, 2003; U.S. Provisional Patent Application No. 60/441,405 filed Jan. 21, 2003; U.S. Provisional Patent Application No. 60/441,447 filed Jan. 21, 2003; U.S. Provisional Patent Application No. 60/441,381 filed Jan. 21, 2003; and U.S. Provisional Patent Application No. 60/392,415 filed Jun. 26, 2002.

[0002] The U.S. Government has certain rights in this invention. The development of this invention was partially funded by the United States Government under a HATCH grant from the United States Department of Agriculture, partially funded by the United States Government with Formula 1433 funds from the United States Department of Agriculture and partially funded by the United States Government under contract DAAD 19-02016 awarded by the Army.

FIELD OF THE INVENTION

[0003] The present invention relates generally to production of multimeric proteins in a transgenic individual, wherein genes encoding the multimeric proteins are operably-linked to signal sequences, or portions of signal sequences.

BACKGROUND OF THE INVENTION

[0004] Methods for producing multimeric proteins in transgenic animals are desirable for a variety of reasons, including the transgenic animal's potential as biological factories to produce multimeric proteins for pharmaceutical, diagnostic and industrial uses. This potential is attractive to the industry due to the inadequate capacity in facilities used for recombinant production of multimeric proteins and the increasing demand by the pharmaceutical industry for use of these facilities. Numerous attempts to produce transgenic animals have met several problems, including low rates of gene incorporation and unstable gene incorporation. Accordingly, improved gene technologies are needed for the development of transgenic animals for the production of multimeric proteins.

[0005] Several of the prior art gene delivery technologies employed viruses that are associated with potentially undesirable side effects and safety concerns. The majority of current gene-delivery technologies useful for gene therapy rely on virus-based delivery vectors, such as adeno and adeno-associated viruses, retroviruses, and other viruses, which have been attenuated to no longer replicate. (Kay, M. A., et al. 2001. Nature Medicine 7:3340).

[0006] There are multiple problems associated with the use of viral vectors. Firstly, they are not tissue-specific. In fact, a gene therapy trial using adenovirus was recently halted because the vector was present in the patient's sperm (Gene trial to proceed despite fears that therapy could change child's genetic makeup. The New York Times, Dec. 23, 2001). Secondly, viral vectors are likely to be transiently incorporated, which necessitates re-treating a patient at specified time intervals. (Kay, M. A., et al. 2001. Nature Medicine 7:33-40). Thirdly, there is a concern that a viral-based vector could revert to its virulent form and cause disease. Fourthly, viral-based vectors require a dividing cell for stable integration. Fifthly, viral-based vectors indiscriminately integrate into various cells, which can result in undesirable germline integration. Sixthly, the required high titers needed to achieve the desired effect have resulted in the death of one patient and they are believed to be responsible for induction of cancer in a separate study. (Science, News of the Week, Oct. 4, 2002).

[0007] Accordingly, what is needed is a new method to produce multimeric proteins in transgenic animals and humans, in which the vector containing those genes does not cause disease or other unwanted side effects. There is also a need for DNA constructs that would be stably incorporated into the tissues and cells of animals and humans, including cells in the resting state that are not replicating. There is a further recognized need in the art for DNA constructs capable of delivering genes to specific tissues and cells of animals and humans and for producing multimeric proteins in those animals and humans.

SUMMARY OF THE INVENTION

[0008] The present invention provides a new, effective and efficient method of producing multimeric proteins in an individual. Multimeric proteins include associated multimeric proteins (two or more associated polypeptides) and multivalent multimeric proteins (a single polypeptide encoded by more than one gene of interest). Expression and/or formation of the multimeric protein in the individual is achieved by administering a polynucleotide cassette containing the genes of interest to the individual. The polynucleotide cassette may additionally contain one or more pro sequences, prepro sequences, cecropin prepro sequences, and/or cleavage site sequences.

[0009] This invention provides polynucleotide cassettes containing two or more genes of interest and two or more pro polynucleotide sequences, wherein each gene of interest is operably-linked to a pro nucleotide sequence. Each of the genes of interest encodes a polypeptide that forms a part of the multimeric protein. One discovery of the present invention is the use of pro portions of prepro signal sequences to facilitate appropriate processing, expression, and/or formation of multimeric proteins in an individual. Several examples of prepro polynucleotides from which a pro polynucleotide can be derived or be a part of are a cecropin prepro, lysozyme prepro, ovomucin prepro, ovotransferrin prepro, a signal peptide for tumor necrosis factor receptor (SEQ ID NO:6), a signal peptide encoded by a polynucleotide sequence provided in one of SEQ ID NOs:7-54 and a signal peptide provide in SEQ ID NO:55. The prepro or pro polynucleotide can be a cecropin prepro or pro polynucleotide selected from the group consisting of cecropin A1, cecropin A2, cecropin B, cecropin C, cecropin D, cecropin E and cecropin F. In a preferred embodiment, the pro polynucleotide is a cecropin B pro polynucleotide having a sequence shown in SEQ ID NO:1 or SEQ ID NO:2. A preferred prepro polynucleotide is a cecropin B polynucleotide having a sequence shown in SEQ ID NO:3 or SEQ ID NO:4.

[0010] Another discovery of the present invention is that cecropin prepro sequences facilitate appropriate processing, expression, and/or formation of proteins, including multimeric proteins, in an individual. Accordingly, the present invention includes polynucleotide cassettes containing one or more genes of interest operably-linked to a cecropin prepro sequence. In one embodiment, the polynucleotide cassette contains two or more genes of interest operably-linked to a cecropin prepro sequence. Preferred cecropin prepro polynucleotides are provided in SEQ ID NO:3 and SEQ ID NO:4. The present invention also includes polynucleotide cassettes containing two or more genes of interest operably linked to a cecropin prepro polynucleotide, wherein pro sequences are located between the genes of interest.

[0011] These polynucleotide cassettes are administered to an individual for expression of polypeptide sequences and the formation of a protein, and more preferably, a multimeric protein. Preferably, the individual is an animal from which the protein can be harvested. Preferred animals are egg-laying or milk-producing animals.

[0012] In one embodiment, the egg-laying transgenic animal is an avian. The method of the present invention may be used in avians including Ratites, Psittaciformes, Falconiformes, Piciformes, Strigiformes, Passeriformes, Coraciformes, Ralliformes, Cuculiformes, Columbiformes, Galliformes, Anseriformes, and Herodiones. Preferably, the egg-laying transgenic animal is a poultry bird. More preferably, the bird is a chicken, turkey, duck, goose or quail. Another preferred bird is a ratite, such as, an emu, an ostrich, a rhea, or a cassowary. Other preferred birds are partridge, pheasant, kiwi, parrot, parakeet, macaw, falcon, eagle, hawk, pigeon, cockatoo, song birds, jay bird, blackbird, finch, warbler, canary, toucan, mynah, or sparrow.

[0013] In some embodiments, the polynucleotide cassettes are located within transposon-based vectors that allow for incorporation of the cassettes into the DNA of the individual. The transposon-based vectors of the present invention include a transposase, operably-linked to a first promoter, and a coding sequence for a protein or peptide of interest operably-linked to a second promoter, wherein the coding sequence for the protein or peptide of interest and its operably-linked promoter are flanked by transposase insertion sequences recognized by the transposase. The transposon-based vector also includes the following characteristics: a) one or more modified Kozak sequences comprising ACCATG (SEQ ID NO:5) at the 3′ end of the first promoter to enhance expression of the transposase; b) modifications of the codons for the first several N-terminal amino acids of the transposase, wherein the nucleotide at the third base position of each codon is changed to an A or a T without changing the corresponding amino acid; c) addition of one or more stop codons to enhance the termination of transposase synthesis; and/or, d) addition of an effective polyA sequence operably-linked to the transposase to further enhance expression of the transposase gene. In some embodiments, the effective polyA sequence is an avian optimized polyA sequence.

[0014] In one embodiment, the transposon-based vector comprises an avian optimized polyA sequence and does not comprise a modified Kozak sequence comprising ACCATG (SEQ ID NO:5). One example of such a transposon-based vector is the pTnMCS vector (SEQ ID NO:56). In another embodiment the transposon-based vector comprises a) one or more modified Kozak sequences comprising ACCATG (SEQ ID NO:5) at the 3′ end of the first promoter to enhance expression of the transposase; b) modifications of the codons for the first several N-terminal amino acids of the transposase, wherein the third base of each codon was changed to an A or a T without changing the corresponding amino acid; c) addition of one or more stop codons to enhance the termination of transposase synthesis; and, d) addition of an effective polyA sequence operably-linked to the transposase to further enhance expression of the transposase gene. One example of such a transposon-based vector is the pTnMod vector (SEQ ID NO:57).

[0015] Accordingly, it is an object of the present invention to provide improved methods for the production of multimeric proteins in an individual.

[0016] It is another object of the present invention to provide improved methods for the production of multimeric proteins in an egg-laying animal or a milk-producing animal.

[0017] It is yet another object of the present invention to provide improved methods for the production of multimeric proteins in a chicken or quail.

[0018] Another object of the present invention is to provide a method to produce an egg or milk containing a multimeric protein.

[0019] An advantage of the present invention is that multimeric proteins are produced by transgenic animals much more efficiently and economically than prior art methods, thereby providing a means for large scale production of multimeric proteins.

[0020] These and other objects, features and advantages of the present invention will become apparent after a review of the following detailed description of the disclosed embodiments and claims.

BRIEF DESCRIPTION OF THE FIGURES

[0021]FIG. 1 depicts schematically a polynucleotide cassette containing two genes of interest operably-linked to two pro polynucleotides, wherein the first pro polynucleotide is a part of a prepro polynucleotide. “Prom” indicates promoter.

[0022]FIG. 2 depicts schematically a polynucleotide cassette containing polynucleotides encoding for a heavy chain and a light chain of an antibody. “Oval prom” indicates an ovalbumin promoter. The polynucleotide cassette contains pro and prepro sequences and is flanked by insertion sequences (IS) recognized by a transposase.

[0023]FIG. 3 depicts schematically a polynucleotide cassette containing a cecropin prepro sequence operably-linked to two genes of interest. Between the genes of interest resides a cleavage site indicates by “CS.”

[0024]FIG. 4 depicts schematically a polynucleotide cassette containing two genes of interest, a promoter (prom), a signal sequence (SS) and a cleavage site (CS). The polynucleotide cassette is flanked by insertion sequences (IS) recognized by a transposase.

[0025]FIG. 5 is a picture of a gel showing partially purified egg white derived from a transgenic avian run under reducing and non-reducing conditions.

DETAILED DESCRIPTION OF THE INVENTION

[0026] The present invention provides a new, effective and efficient method of producing multimeric proteins in an individual. Multimeric proteins include associated multimeric proteins (two or more associated polypeptides) and multivalent multimeric proteins (a single polypeptide encoded by more than one gene of interest). Expression and/or formation of the multimeric protein in the individual is achieved by administering a polynucleotide cassette containing the genes of interest to the individual. The polynucleotide cassette may additionally contain one or more pro sequences, prepro sequences, cecropin prepro sequences, and/or cleavage site sequences.

[0027] This invention provides polynucleotide cassettes containing two or more genes of interest and two or more pro polynucleotide sequences, wherein each gene of interest is operably-linked to a pro nucleotide sequence. Each of the genes of interest encodes a polypeptide that forms a part of the multimeric protein. These polynucleotide cassettes are administered to an individual for expression of the polypeptide sequences and expression and/or formation of the multimeric protein. Preferably, the individual is an animal from which the multimeric protein can be harvested. Preferred animals are egg-laying or milk-producing animals. In some embodiments, the polynucleotide cassettes are located within transposon-based vectors that allow for incorporation of the cassettes into the DNA of the individual.

[0028] The pro polynucleotide sequences operably-linked to the genes of interest include pro portions of prepro polynucleotide sequences commonly associated with polynucleotides encoding proteins secreted from a cell in nature. It may be that the pre polynucleotide sequence functions to direct the resultant protein into the endoplasmic reticulum and the pro sequence is cleaved within the endoplasmic reticulum or Golgi complex of a cell containing the protein. While prepro polynucleotide sequences are associated with secreted polypeptides in nature, one discovery of the present invention is the use of pro portions of the prepro signal sequences to facilitate appropriate processing, expression, and/or formation of multimeric proteins, and more particularly, associated multimeric proteins. In the present invention, each gene of interest is operably-linked with a pro polynucleotide sequence. FIG. 1 shows schematically one polynucleotide cassette containing two genes of interest, wherein each gene of interest is operably-linked to a pro polynucleotide sequence. The first gene of interest is operably-linked to a pro polynucleotide sequence that is part of a prepro polynucleotide sequence, while the second gene of interest is operably-linked to a pro polynucleotide sequence that is not part of a prepro polynucleotide sequence, but may have been derived from a prepro polynucleotide sequence. Accordingly, the term “pro sequence” encompasses a pro sequence that is part of a prepro sequence and a pro sequence that is not part of a prepro sequence, but may have been derived from a prepro sequence. In preferred embodiments, the most 5′ pro polynucleotide sequence in the polynucleotide cassette is a part of a prepro polynucleotide sequence.

[0029] Several examples of prepro polynucleotides from which a pro polynucleotide can be derived or be a part of are a cecropin prepro, lysozyme prepro, ovomucin prepro, ovotransferrin prepro, a signal peptide for tumor necrosis factor receptor (SEQ ID NO:6), a signal peptide encoded by a polynucleotide sequence provided in one of SEQ ID NOs:7-54 and a signal peptide provide in SEQ ID NO:55. The prepro or pro polynucleotide can be a cecropin prepro or pro polynucleotide selected from the group consisting of cecropin A1, cecropin A2, cecropin B, cecropin C, cecropin D, cecropin E and cecropin F. In a preferred embodiment, the pro polynucleotide is a cecropin B pro polynucleotide having a sequence shown in SEQ ID NO:1 or SEQ ID NO:2. A preferred prepro polynucleotide is a cecropin B polynucleotide having a sequence shown in SEQ ID NO:3 or SEQ ID NO:4.

[0030]FIG. 1 provides one embodiment of the invention wherein the polynucleotide cassette includes two genes of interest and two pro polynucleotide sequences arranged in the following order: a prepro polynucleotide, a first gene of interest, a pro polynucleotide, and a second gene of interest. Preferably, the sequences are arranged in the aforementioned order beginning at a 5′ end of the polynucleotide cassette. FIG. 2 provides a more specific embodiment of the present invention wherein the first and second genes of interest are polynucleotides encoding antibody heavy and light chains. However, the invention includes polynucleotide cassettes containing at least two genes of interest. Each of the genes of interest is operably-linked to a pro polynucleotide. Each of these pro polynucleotides can be the same, or each can be different. In one embodiment, all of the pro polynucleotides in the polynucleotide cassette are the same and are cecropin pro polynucleotides. The most 5′ cecropin pro polynucleotide is preferably a part of a cecropin prepro polynucleotide sequence as shown in FIG. 3.

[0031] The polynucleotide cassettes of the present invention may be administered to an individual for production of a multimeric protein in that individual. Accordingly, the present invention includes a method of producing a multimeric protein in an individual comprising administering to the individual a polynucleotide cassette comprising at least two genes of interest, each encoding a part of the multimeric protein, wherein each gene of interest is operably-linked to a pro polynucleotide sequence. The present invention also includes a method of producing a multimeric protein in an individual comprising administering to the individual a polynucleotide cassette comprising a cecropin prepro sequence operably-linked to two or more genes of interest, each gene of interest encoding a part of the multimeric protein. This second method does not require the linking of pro polynucleotides to each gene of interest since the use of a cecropin prepro sequence itself in a polynucleotide cassette facilitates processing, expression, and/or formation of multimeric proteins. Polynucleotide cassettes containing the cecropin prepro polynucleotide can contain at least two genes of interest. Preferably, the cecropin prepro polynucleotide is located 5′ of the genes of interest in the polynucleotide cassette. One exemplary polynucleotide cassette is shown in FIG. 3. In a preferred embodiment, the prepro sequence comprises a sequence shown in SEQ ID NO:3 or SEQ ID NO:4. As shown in FIG. 3, the polynucleotide cassettes containing a cecropin prepro polynucleotide preferably contain a cleavage site between each of two genes of interest. Such cleavage site(s) may be nucleotides encoding any cleavage sites including, but not limited to, an enzymatic cleavage site, a pro polynucleotide, and a photolabile cleavage site, a chemical cleavage site, and a self-splicing cleavage site (i.e., intein). Cleavage sites are discussed in more detail below.

[0032] The polynucleotide cassettes of the present invention are particularly suited for production of multimeric proteins in an individual. Individuals include both humans and animals. Preferred animals are egg-laying animals and milk-producing animals. As used herein, the term “egg-laying animal” includes all amniotes such as birds, turtles, lizards and monotremes. Monotremes are egg-laying mammals and include the platypus and echidna. The term “bird” or “fowl,” as used herein, is defined as a member of the Aves class of animals which are characterized as warm-blooded, egg-laying vertebrates primarily adapted for flying. Avians include, without limitation, Ratites, Psittaciformes, Falconiformes, Piciformes, Strigiformes, Passeriformes, Coraciformes, Ralliformes, Cuculiformes, Columbiformes, Galliformes, Anseriformes, and Herodiones. The term “Ratite,” as used herein, is defined as a group of flightless, mostly large, running birds comprising several orders and including the emus, ostriches, kiwis, and cassowaries. The term “Psittaciformes”, as used herein, includes parrots and refers to a monofamilial order of birds that exhibit zygodactylism and have a strong hooked bill. A “parrot” is defined as any member of the avian family Psittacidae (the single family of the Psittaciformes), distinguished by the short, stout, strongly hooked beak. Preferred avians are poultry birde including chickens, quail, turkeys, geese and ducks. The term “chicken” as used herein denotes chickens used for table egg production, such as egg-type chickens, chickens reared for public meat consumption, or broilers, and chickens reared for both egg and meat production (“dual-purpose” chickens). The term “chicken” also denotes chickens produced by primary breeder companies, or chickens that are the parents, grandparents, great-grandparents, etc. of those chickens reared for public table egg, meat, or table egg and meat consumption.

[0033] When the polynucleotide cassettes of the present invention are administered to an egg-laying or milk-producing animal, a transgenic animal containing a polynucleotide cassette is created and the animal produces a transgenic multimeric protein. It is preferred that the resultant multimeric protein is deposited in the egg or in the milk. Various different signal sequences and promoters may be used to achieve deposition of the multimeric protein in the egg or in the milk and these are described in more detail below. In order to achieve a transgenic animal containing a polynucleotide cassette of the present invention, the polynucleotide cassettes can be administered to the individual with, or contained in, any vector, as naked DNA, or in any delivery construct or solution. A preferred vector for incorporation of the polynucleotide cassettes into an individual is a transposon-based vector described below.

[0034] Definitions

[0035] It is to be understood that as used in the specification and in the claims, “a” or “an” can mean one or more, depending upon the context in which it is used. Thus, for example, reference to “a cell” can mean that at least one cell can be utilized.

[0036] The term “antibody” is used interchangeably with the term “immunoglobulin” and is defined herein as a protein synthesized by an animal or a cell of the immune system in response to the presence of a foreign substance commonly referred to as an “antigen” or an “immunogen”. The term antibody includes fragments of antibodies. Antibodies are characterized by specific affinity to a site on the antigen, wherein the site is referred to an “antigenic determinant” or an “epitope”. Antigens can be naturally occurring or artificially engineered. Artificially engineered antigens include but are not limited to small molecules, such as small peptides, attached to haptens such as macromolecules, for example proteins, nucleic acids, or polysaccharides. Artificially designed or engineered variants of naturally occurring antibodies and artificially designed or engineered antibodies not occurring in nature are all included in the current definition. Such variants include conservatively substituted amino acids and other forms of substitution as described in the section concerning proteins and polypeptides.

[0037] The term “egg” is defined herein as including a large female sex cell enclosed in a porous, calcarous or leathery shell, produced by birds and reptiles. The term “ovum” is defined as a female gamete, and is also known as an egg. Therefore, egg production in all animals other than birds and reptiles, as used herein, is defined as the production and discharge of an ovum from an ovary, or “ovulation”. Accordingly, it is to be understood that the term “egg” as used herein is defined as a large female sex cell enclosed in a porous, calcarous or leathery shell, when a bird or reptile produces it, or it is an ovum when it is produced by all other animals.

[0038] The term “gene” is defined herein to include a polynucleotide that includes a coding region for a protein, peptide or polypeptide, with or without intervening sequences such as introns.

[0039] The term “multimeric protein” is defined herein to include one or more polypeptides that are associated, or joined, by any means including disulfde bonds. An example of this type of multimeric protein is an antibody that contains both heavy and light chains that are associated by disulfide bonds. These multimeric proteins are referred to herein as “associated multimeric proteins.” The term “multimeric protein” also includes a polypeptide that is encoded by more than one gene of interest. An example of this type of multimeric protein is a single polypeptide containing a heavy chain polypeptide (first polypeptide of interest) and a light chain polypeptide (second polypeptide of interest). In these embodiments, the different polypeptides of interest may be separated by other polypeptide sequences such as spacer polypeptides and cleavage site polypeptides. These types of multimeric proteins are referred to herein as “multivalent multimeric proteins.”

[0040] The term “milk-producing animal” refers herein to mammals including, but not limited to, bovine, ovine, porcine, equine, and primate animals. Milk-producing animals include but are not limited to cows, llamas, camels, goats, reindeer, zebu, water buffalo, yak, horses, pigs, rabbits, non-human primates, and humans.

[0041] The term “transgenic animal” refers to an animal having at least a portion of the transposon-based vector DNA is incorporated into its DNA. While a transgenic animal includes an animal wherein the transposon-based vector DNA is incorporated into the germline DNA, a transgenic animal also includes an animal having DNA in one or more somatic cells that contain a portion of the transposon-based vector DNA for any period of time. In a preferred embodiment, a portion of the transposon-based vector comprises a gene of interest. More preferably, the gene of interest is incorporated into the animal's DNA for a period of at least five days, more preferably the laying life of the animal, and most preferably the life of the animal. In a further preferred embodiment, the animal is an avian.

[0042] The term “vector” is used interchangeably with the terms “construct”, “DNA construct” and “genetic construct” to denote synthetic nucleotide sequences used for manipulation of genetic material, including but not limited to cloning, subcloning, sequencing, or introduction of exogenous genetic material into cells, tissues or organisms, such as birds. It is understood by one skilled in the art that vectors may contain synthetic DNA sequences, naturally occurring DNA sequences, or both. The vectors of the present invention are transposon-based vectors as described herein.

[0043] When referring to two nucleotide sequences, one being a regulatory sequence, the term “operably-linked” is defined herein to mean that the two sequences are associated in a manner that allows the regulatory sequence to affect expression of the other nucleotide sequence. It is not required that the operably-linked sequences be directly adjacent to one another with no intervening sequence(s).

[0044] The term “regulatory sequence” is defined herein as including promoters, enhancers and other expression control elements such as polyadenylation sequences, matrix attachment sites, insulator regions for expression of multiple genes on a single construct, ribosome entry/attachment sites, introns that are able to enhance expression, and silencers.

[0045] Transposon-Based Vectors

[0046] While not wanting to be bound by the following statement, it is believed that the nature of the DNA construct is an important factor in successfully producing transgenic animals. The “standard” types of plasmid and viral vectors that have previously been almost universally used for transgenic work in all species, especially avians, have low efficiencies and may constitute a major reason for the low rates of transformation previously observed. The DNA (or RNA) constructs previously used often do not integrate into the host DNA, or integrate only at low frequencies. Other factors may have also played a part, such as poor entry of the vector into target cells. The present invention provides transposon-based vectors that can be administered to an animal that overcome the prior art problems relating to low transgene integration frequencies. Two preferred transposon-based vectors of the present invention in which a transposase, gene of interest and other polynucleotide sequences may be introduced are termed pTnMCS (SEQ ID NO:56) and pTnMod (SEQ ID NO:57).

[0047] The transposon-based vectors of the present invention produce integration frequencies an order of magnitude greater than has been achieved with previous vectors. More specifically, intratesticular injections performed with a prior art transposon-based vector (described in U.S. Pat. No. 5,719,055) resulted in 41% sperm positive roosters whereas intratesticular injections performed with the novel transposon-based vectors of the present invention resulted in 77% sperm positive roosters. Actual frequencies of integration were estimated by either or both comparative strength of the PCR signal from the sperm and histological evaluation of the testes and sperm by quantitative PCR.

[0048] The transposon-based vectors of the present invention include a transposase gene operably-linked to a first promoter, and a coding sequence for a desired protein or peptide operably-linked to a second promoter, wherein the coding sequence for the desired protein or peptide and its operably-linked promoter are flanked by transposase insertion sequences recognized by the transposase. The transposon-based vector also includes one or more of the following characteristics: a) one or more modified Kozak sequences comprising ACCATG (SEQ ID NO:5) at the 3′ end of the first promoter to enhance expression of the transposase; b) modifications of one or more of the codons for the first several N-terminal amino acids of the transposase, wherein the third base of each codon was changed to an A or a T without changing the corresponding amino acid; c) addition of one or more stop codons to enhance the termination of transposase synthesis; and/or, d) addition of an effective polyA sequence operably-linked to the transposase to further enhance expression of the transposase gene. In one embodiment, the transposon-based vector comprises an avian optimized polyA sequence and does not comprise a modified Kozak sequence comprising ACCATG (SEQ ID NO:5). One example of such a transposon-based vector is the pTnMCS vector (SEQ ID NO:56). In another embodiment the transposon-based vector comprises a) one or more modified Kozak sequences comprising ACCATG (SEQ ID NO:5) at the 3′ end of the first promoter to enhance expression of the transposase; b) modifications of the codons for the first several N-terminal amino acids of the transposase, wherein the third base of each codon was changed to an A or a T without changing the corresponding amino acid; c) addition of one or more stop codons to enhance the termination of transposase synthesis; and, d) addition of an effective polyA sequence operably-linked to the transposase to further enhance expression of the transposase gene. One example of such a transposon-based vector is the pTnMod vector (SEQ ID NO:57). The transposon-based vector may additionally or alternatively include one or more of the following Kozak sequences at the 3′ end of any promoter, including the promoter operably-linked to the transposase: ACCATGG (SEQ ID NO:58), AAGATGT (SEQ ID NO:59), ACGATGA (SEQ ID NO:60), AAGATGG (SEQ ID NO:61), GACATGA (SEQ ID NO:62), ACCATGA (SEQ ID NO:63), and ACCATGA (SEQ ID NO:64), ACCATGT (SEQ ID NO:65).

[0049] Transposases and Insertion Sequences

[0050] In a further embodiment of the present invention, the transposase found in the transposase-based vector is an altered target site (ATS) transposase and the insertion sequences are those recognized by the ATS transposase. However, the transposase located in the transposase-based vectors is not limited to a modified ATS transposase and can be derived from any transposase. Transposases known in the prior art include those found in AC7, Tn5SEQ1, Tn916, Tn951, Tn1721, Tn2410, Tn1681, Tn1, Tn2, Tn3, Tn4, Tn5, Tn6, Tn9, Tn10, Tn30, Tn101, Tn903, Tn501, Tn1000 (γδ), Tn1681, Tn2901, AC transposons, Mp transposons, Spm transposons, En transposons, Dotted transposons, Mu transposons, Ds transposons, dSpm transposons and I transposons. According to the present invention, these transposases and their regulatory sequences are modified for improved functioning as follows: a) the addition one or more modified Kozak sequences comprising ACCATG (SEQ ID NO:5) at the 3′ end of the promoter operably-linked to the transposase; b) a change of one or more of the codons for the first several amino acids of the transposase, wherein the third base of each codon was changed to an A or a T without changing the corresponding amino acid; c) the addition of one or more stop codons to enhance the termination of transposase synthesis; and/or, d) the addition of an effective polyA sequence operably-linked to the transposase to further enhance expression of the transposase gene.

[0051] Although not wanting to be bound by the following statement, it is believed that the modifications of the first several N-terminal codons of the transposase gene facilitate transcription of the transposase gene, in part, by increasing strand dissociation during transcription. It is preferable that one or more of between approximately the first 1 to 20, more preferably 3 to 15, and most preferably between 4 to 12 N-terminal codons of the transposase are modified such that the third base of each codon is changed to an A or a T without changing the encoded amino acid. In one embodiment, the first ten N-terminal codons of the transposase gene are modified in this manner. It is also preferred that the transposase contain mutations that make it less specific for preferred insertion sites and thus increases the rate of transgene insertion as discussed in U.S. Pat. No. 5,719,055.

[0052] In some embodiments, the transposon-based vectors are optimized for expression in a particular host by changing the methylation patterns of the vector DNA. For example, prokaryotic methylation may be reduced by using a methylation deficient organism for production of the transposon-based vector. The transposon-based vectors may also be methylated to resemble eukaryotic DNA for expression in a eukaryotic host.

[0053] Transposases and insertion sequences from other analogous eukaryotic transposon-based vectors that can also be modified and used are, for example, the Drosophila P element derived vectors disclosed in U.S. Pat. No. 6,291,243; the Drosophila mariner element described in Sherman et al. (1998); or the sleeping beauty transposon. See also Hackett et al. (1999); D. Lampe et al., 1999. Proc. Natl. Acad. Sci. USA, 96:11428-11433; S. Fischer et al., 2001. Proc. Natl. Acad. Sci. USA, 98:6759-6764; L. Zagoraiou et al., 2001. Proc. Natl. Acad. Sci. USA, 98:11474-11478; and D. Berg et al. (Eds.), Mobile DNA, Amer. Soc. Microbiol. (Washington, D.C., 1989). However, it should be noted that bacterial transposon-based elements are preferred, as there is less likelihood that a eukaryotic transposase in the recipient species will recognize prokaryotic insertion sequences bracketing the transgene.

[0054] Many transposases recognize different insertion sequences, and therefore, it is to be understood that a transposase-based vector will contain insertion sequences recognized by the particular transposase also found in the transposase-based vector. In a preferred embodiment of the invention, the insertion sequences have been shortened to about 70 base pairs in length as compared to those found in wild-type transposons that typically contain insertion sequences of well over 100 base pairs.

[0055] While the examples provided below incorporate a “cut and insert” Tn10 based vector that is destroyed following the insertion event, the present invention also encompasses the use of a “rolling replication” type transposon-based vector. Use of a rolling replication type transposon allows multiple copies of the transposon/transgene to be made from a single transgene construct and the copies inserted. This type of transposon-based system thereby provides for insertion of multiple copies of a transgene into a single genome. A rolling replication type transposon-based vector may be preferred when the promoter operably-linked to gene of interest is endogenous to the host cell and present in a high copy number or highly expressed. However, use of a rolling replication system may require tight control to limit the insertion events to non-lethal levels. Tn1, Tn2, Tn3, Tn4, Tn5, Tn9, Tn21, Tn501, Tn551, Tn951, Tn1721, Tn2410 and Tn2603 are examples of a rolling replication type transposon, although Tn5 could be both a rolling replication and a cut and insert type transposon.

[0056] Stop Codons and PolyA Sequences

[0057] In one embodiment, the transposon-based vector contains two stop codons operably-linked to the transposase and/or to the gene of interest. In an alternate embodiment, one stop codon of UAA or UGA is operably linked to the transposase and/or to the gene of interest. While not wanting to be bound by the following statement, it is thought that the stop codon UAG is less effective in translation termination and is therefore less desirable in the constructs described herein.

[0058] As used herein an “effective polyA sequence” refers to either a synthetic or non-synthetic sequence that contains multiple and sequential nucleotides containing an adenine base (an A polynucleotide string) and that increases expression of the gene to which it is operably-linked. A polyA sequence may be operably-linked to any gene in the transposon-based vector including, but not limited to, a transposase gene and a gene of interest. A preferred polyA sequence is optimized for use in the host animal or human. In one embodiment, the polyA sequence is optimized for use in an avian species and more specifically, a chicken. An avian optimized polyA sequence generally contains a minimum of 40 base pairs, preferably between approximately 40 and several hundred base pairs, and more preferably approximately 75 base pairs that precede the A polynucleotide string and thereby separate the stop codon from the A polynucleotide string. In one embodiment of the present invention, the polyA sequence comprises a conalbumin polyA sequence as provided in SEQ ID NO:66 and as taken from GenBank accession # Y00407, base pairs 10651-11058. In another embodiment, the polyA sequence comprises a synthetic polynucleotide sequence shown in SEQ ID NO:67. In yet another embodiment, the polyA sequence comprises an avian optimized polyA sequence provided in SEQ ID NO:68. A chicken optimized polyA sequence may also have a reduced amount of CT repeats as compared to a synthetic polyA sequence.

[0059] It is a surprising discovery of the present invention that such an avian optimized poly A sequence increases expression of a polynucleotide to which it is operably-linked in an avian as compared to a non-avian optimized polyA sequence. Accordingly, the present invention includes methods of or increasing incorporation of a gene of interest wherein the gene of interest resides in a transposon-based vector containing a transposase gene and wherein the transposase gene is operably linked to an avian optimized polyA sequence. The present invention also includes methods of increasing expression of a gene of interest in an avian that includes administering a gene of interest to the avian, wherein the gene of interest is operably-linked to an avian optimized polyA sequence. An avian optimized polyA nucleotide string is defined herein as a polynucleotide containing an A polynucleotide string and a minimum of 40 base pairs, preferably between approximately 40 and several hundred base pairs, and more preferably approximately 75 base pairs that precede the A polynucleotide string. The present invention further provides transposon-based vectors containing a gene of interest or transposase gene operably linked to an avian optimized polyA sequence.

[0060] Promoters and Enhancers

[0061] The first promoter operably-linked to the transposase gene and the second promoter operably-linked to the gene of interest can be a constitutive promoter or an inducible promoter. Constitutive promoters include, but are not limited to, immediate early cytomegalovirus (CMV) promoter, herpes simplex virus 1 (HSV1) immediate early promoter, SV40 promoter, lysozyme promoter, early and late CMV promoters, early and late HSV promoters, β-actin promoter, tubulin promoter, Rous-Sarcoma virus (RSV) promoter, and heat-shock protein (HSP) promoter. Inducible promoters include tissue-specific promoters, developmentally-regulated promoters and chemically inducible promoters. Examples of tissue-specific promoters include the glucose 6 phosphate (G6P) promoter, vitellogenin promoter, ovalbumin promoter, ovomucoid promoter, conalbumin promoter, ovotransferrin promoter, prolactin promoter, kidney uromodulin promoter, and placental lactogen promoter. In one embodiment, the vitellogenin promoter includes a polynucleotide sequence of SEQ ID NO:69. The G6P promoter sequence may be deduced from a rat G6P gene untranslated upstream region provided in GenBank accession number U57552.1. Examples of developmentally-regulated promoters include the homeobox promoters and several hormone induced promoters. Examples of chemically inducible promoters include reproductive hormone induced promoters and antibiotic inducible promoters such as the tetracycline inducible promoter and the zinc-inducible metallothionine promoter.

[0062] Other inducible promoter systems include the Lac operator repressor system inducible by IPTG (isopropyl beta-D-thiogalactoside) (Cronin, A. et al. 2001. Genes and Development, v. 15), ecdysone-based inducible systems (Hoppe, U. C. et al. 2000. Mol. Ther. 1:159-164); estrogen-based inducible systems (Braselmann, S. et al. 1993. Proc. Natl. Acad. Sci. 90:1657-1661); progesterone-based inducible systems using a chimeric regulator, GLVP, which is a hybrid protein consisting of the GAL4 binding domain and the herpes simplex virus transcriptional activation domain, VP16, and a truncated form of the human progesterone receptor that retains the ability to bind ligand and can be turned on by RU486 (Wang, et al. 1994. Proc. Natl. Acad. Sci. 91:8180-8184); CID-based inducible systems using chemical inducers of dimerization (CIDs) to regulate gene expression, such as a system wherein rapamycin induces dimerization of the cellular proteins FKBP12 and FRAP (Belshaw, P. J. et al. 1996. J. Chem. Biol. 3:731-738; Fan, L. et al. 1999. Hum. Gene Ther. 10:2273-2285; Shariat, S. F. et al. 2001. Cancer Res. 61:2562-2571; Spencer, D. M. 1996. Curr. Biol. 6:839-847). Chemical substances that activate the chemically inducible promoters can be administered to the animal containing the transgene of interest via any method known to those of skill in the art.

[0063] Other examples of cell or tissue-specific and constitutive promoters include but are not limited to smooth-muscle SM22 promoter, including chimeric SM22alpha/telokin promoters (Hoggatt A. M. et al., 2002. Circ Res. 91(12):1151-9); ubiquitin C promoter (Biochim Biophys Acta, 2003. Jan. 3; 1625(1):52-63); Hsf2 promoter; murine COMP (cartilage oligomeric matrix protein) promoter; early B cell-specific mb-1 promoter (Sigvardsson M., et al., 2002. Mol. Cell Biol. 22(24):8539-51); prostate specific antigen (PSA) promoter (Yoshimura I. et al., 2002, J. Urol. 168(6):2659-64); exorh promoter and pineal expression-promoting element (Asaoka Y., et al., 2002. Proc. Natl. Acad. Sci. 99(24):15456-61); neural and liver ceramidase gene promoters (Okino N. et al., 2002. Biochem. Biophys. Res. Commun. 299(1):160-6); PSP94 gene promoter/enhancer (Gabril M. Y. et al., 2002. Gene Ther. 9(23):1589-99); promoter of the human FAT/CD36 gene (Kuriki C., et al., 2002. Biol. Pharm. Bull. 25(11):1476-8); VL30 promoter (Staplin W. R. et al., 2002. Blood Oct. 24, 2002); and IL-10 promoter (Brenner S., et al., 2002. J. Biol. Chem. Dec. 18, 2002).

[0064] Examples of avian promoters include, but are not limited to, promoters controlling expression of egg white proteins, such as ovalbumin, ovotransferrin (conalbumin), ovomucoid, lysozyme, ovomucin, g2 ovoglobulin, g3 ovoglobulin, ovoflavoprotein, ovostatin (ovomacroglobin), cystatin, avidin, thiamine-binding protein, glutamyl aminopeptidase minor glycoprotein 1, minor glycoprotein 2; and promoters controlling expression of egg-yolk proteins, such as vitellogenin, very low-density lipoproteins, low density lipoprotein, cobalamin-binding protein, riboflavin-binding protein, biotin-binding protein (Awade, 1996. Z. Lebensm. Unters. Forsch. 202:1-14). An advantage of using the vitellogenin promoter is that it is active during the egg-laying stage of an animal's life-cycle, which allows for the production of the protein of interest to be temporally connected to the import of the protein of interest into the egg yolk when the protein of interest is equipped with an appropriate targeting sequence. In some embodiments, the avian promoter is an oviduct-specific promoter. As used herein, the term “oviduct-specific promoter” includes, but is not limited to, ovalbumin, ovotransferrin (conalbumin), ovomucoid, lysozyme, ovomucin, g2 ovoglobulin, g3 ovoglobulin, ovoflavoprotein, and ovostatin (ovomacroglobin) promoters.

[0065] Liver-specific promoters of the present invention include, but are not limited to, the following promoters, vitellogenin promoter, G6P promoter, cholesterol-7-alpha-hydroxylase (CYP7A) promoter, phenylalanine hydroxylase (PAH) promoter, protein C gene promoter, insulin-like growth factor I (IGF-I) promoter, bilirubin UDP-glucuronosyltransferase promoter, aldolase B promoter, furin promoter, metallothioneine promoter, albumin promoter, and insulin promoter.

[0066] Also included in the present invention are promoters that can be used to target expression of a protein of interest into the milk of a milk-producing animal including, but not limited to, β lactoglobin promoter, whey acidic protein promoter, lactalbumin promoter and casein promoter.

[0067] Promoters associated with cells of the immune system may also be used. Acute phase promoters such as interleukin (IL)-1 and IL-2 may be employed. Promoters for heavy and light chain Ig may also be employed. The promoters of the T cell receptor components CD4 and CD8, B cell promoters and the promoters of CR2 (complement receptor type 2) may also be employed. Immune system promoters are preferably used when the desired protein is an antibody protein.

[0068] Also included in this invention are modified promoters/enhancers wherein elements of a single promoter are duplicated, modified, or otherwise changed. In one embodiment, a steroid hormone-binding domain of the ovalbumin promoter is moved from about −6.5 kb to within approximately the first 1000 base pairs of the gene of interest. Modifying an existing promoter with promoter/enhancer elements not found naturally in the promoter, as well as building an entirely synthetic promoter, or drawing promoter/enhancer elements from various genes together on a non-natural backbone, are all encompassed by the current invention.

[0069] Accordingly, it is to be understood that the promoters contained within the transposon-based vectors of the present invention may be entire promoter sequences or fragments of promoter sequences. For example, in one embodiment, the promoter operably linked to a gene of interest is an approximately 900 base pair fragment of a chicken ovalbumin promoter (SEQ ID NO:70). The constitutive and inducible promoters contained within the transposon-based vectors may also be modified by the addition of one or more modified Kozak sequences of ACCATG (SEQ ID NO:5).

[0070] As indicated above, the present invention includes transposon-based vectors containing one or more enhancers. These enhancers may or may not be operably-linked to their native promoter and may be located at any distance from their operably-linked promoter. A promoter operably-linked to an enhancer is referred to herein as an “enhanced promoter.” The enhancers contained within the transposon-based vectors are preferably enhancers found in birds, and more preferably, an ovalbumin enhancer, but are not limited to these types of enhancers. In one embodiment, an approximately 675 base pair enhancer element of an ovalbumin promoter is cloned upstream of an ovalbumin promoter with 300 base pairs of spacer DNA separating the enhancer and promoter. In one embodiment, the enhancer used as a part of the present invention comprises base pairs 1-675 of a Chicken Ovalbumin enhancer from GenBank accession #S82527.1. The polynucleotide sequence of this enhancer is provided in SEQ ID NO:71.

[0071] Also included in some of the transposon-based vectors of the present invention are cap sites and fragments of cap sites. In one embodiment, approximately 50 base pairs of a 5′ untranslated region wherein the capsite resides are added on the 3′ end of an enhanced promoter or promoter. An exemplary 5′ untranslated region is provided in SEQ ID NO:72. A putative cap-site residing in this 5′ untranslated region preferably comprises the polynucleotide sequence provided in SEQ ID NO: 73.

[0072] In one embodiment of the present invention, the first promoter operably-linked to the transposase gene is a constitutive promoter and the second promoter operably-linked to the gene of interest is a tissue-specific promoter. In the second embodiment, use of the first constitutive promoter allows for constitutive activation of the transposase gene and incorporation of the gene of interest into virtually all cell types, including the germline of the recipient animal. Although the gene of interest is incorporated into the germline generally, the gene of interest is only expressed in a tissue-specific manner. A transposon-based vector having a constitutive promoter operably-linked to the transposase gene can be administered by any route, and in one embodiment, the vector is administered to an ovary or to an artery leading to the ovary. In another embodiment, the vector is administered into the lumen of the oviduct or into an artery supplying the oviduct.

[0073] It should be noted that cell- or tissue-specific expression as described herein does not require a complete absence of expression in cells or tissues other than the preferred cell or tissue. Instead, “cell-specific” or “tissue-specific” expression refers to a majority of the expression of a particular gene of interest in the preferred cell or tissue, respectively.

[0074] When incorporation of the gene of interest into the germline is not preferred, the first promoter operably-linked to the transposase gene can be a tissue-specific promoter. For example, transfection of a transposon-based vector containing a transposase gene operably-linked to an oviduct specific promoter such as the ovalbumin promoter provides for activation of the transposase gene and incorporation of the gene of interest in the cells of the oviduct but not into the germline and other cells generally. In this embodiment, the second promoter operably-linked to the gene of interest can be a constitutive promoter or an inducible promoter. In a preferred embodiment, both the first promoter and the second promoter are an ovalbumin promoter. In embodiments wherein tissue-specific expression or incorporation is desired, it is preferred that the transposon-based vector is administered directly to the tissue of interest or to an artery leading to the tissue of interest. In a preferred embodiment, the tissue of interest is the oviduct and administration is achieved by direct injection into the lumen of the oviduct or an artery leading to the oviduct. In a further preferred embodiment, administration is achieved by direct injection into the lumen of the magnum or the infundibulum of the oviduct.

[0075] Accordingly, cell specific promoters may be used to enhance transcription in selected tissues. In birds, for example, promoters that are found in cells of the fallopian tube, such as ovalbumin, conalbumin, ovomucoid and/or lysozyme, are used in the vectors to ensure transcription of the gene of interest in the epithelial cells and tubular gland cells of the fallopian tube, leading to synthesis of the desired protein encoded by the gene and deposition into the egg white. In mammals, promoters specific for the epithelial cells of the alveoli of the mammary gland, such as prolactin, insulin, beta lactoglobin, whey acidic protein, lactalbumin, casein, and/or placental lactogen, are used in the design of vectors used for transfection of these cells for the production of desired proteins for deposition into the milk. In liver cells, the G6P promoter may be employed to drive transcription of the gene of interest for protein production. Proteins made in the liver of birds may be delivered to the egg yolk.

[0076] In order to achieve higher or more efficient expression of the transposase gene, the promoter and other regulatory sequences operably-linked to the transposase gene may be those derived from the host. These host specific regulatory sequences can be tissue specific as described above or can be of a constitutive nature. For example, an avian actin promoter and its associated polyA sequence can be operably-linked to a transposase in a transposase-based vector for transfection into an avian. Examples of other host specific promoters that could be operably-linked to the transposase include the myosin and DNA or RNA polymerase promoters.

[0077] Directing Sequences

[0078] In some embodiments of the present invention, the gene of interest is operably-linked to a directing sequence or a sequence that provides proper conformation to the desired protein encoded by the gene of interest. As used herein, the term “directing sequence” refers to both signal sequences and targeting sequences. An egg directing sequence includes, but is not limited to, an ovomucoid signal sequence, an ovalbumin signal sequence, a cecropin prepro sequence, and a vitellogenin targeting sequence. The term “signal sequence” refers to an amino acid sequence, or the polynucleotide sequence that encodes the amino acid sequence, a portion or the entirety of which directs the protein to which it is linked to the endoplasmic reticulum in a eukaryote, and more preferably the translocational pores in the endoplasmic reticulum, or the plasma membrane in a prokaryote, or mitochondria, such as for the purpose of gene therapy for mitochondrial diseases. Signal and targeting sequences can be used to direct a desired protein into, for example, the milk, when the transposon-based vectors are administered to a milk-producing animal.

[0079] Signal sequences can also be used to direct a desired protein into, for example, a secretory pathway for incorporation into the egg yolk or the egg white, when the transposon-based vectors are administered to a bird or other egg-laying animal. The present invention also includes a gene of interest operably-linked to a second gene containing a signal sequence. An example of such an embodiment is wherein the gene of interest is operably-linked to the ovalbumin gene that contains an ovalbumin signal sequence. Other signal sequences that can be included in the transposon-based vectors include, but are not limited to the ovotransferrin and lysozyme signal sequences. In one embodiment, the signal sequence is an ovalbumin signal sequence including a sequence shown in SEQ ID NO:74. In another embodiment, the signal sequence is a shortened ovalbumin signal sequence including a sequence shown in SEQ ID NO:75 or SEQ ID NO:76.

[0080] As also used herein, the term “targeting sequence” refers to an amino acid sequence, or the polynucleotide sequence encoding the amino acid sequence, which amino acid sequence is recognized by a receptor located on the exterior of a cell. Binding of the receptor to the targeting sequence results in uptake of the protein or peptide operably-linked to the targeting sequence by the cell. One example of a targeting sequence is a vitellogenin targeting sequence that is recognized by a vitellogenin receptor (or the low density lipoprotein receptor) on the exterior of an oocyte. In one embodiment, the vitellogenin targeting sequence includes the polynucleotide sequence of SEQ ID NO:77. In another embodiment, the vitellogenin targeting sequence includes all or part of the vitellogenin gene. Other targeting sequences include VLDL and Apo E, which are also capable of binding the vitellogenin receptor. Since the ApoE protein is not endogenously expressed in birds, its presence may be used advantageously to identify birds carrying the transposon-based vectors of the present invention.

[0081] Genes of Interest

[0082] The genes of interest in the polynucleotide cassette can be any gene, and preferably are genes that encode portions of multimeric proteins. A gene of interest may contain modifications of the codons for the first several N-terminal amino acids of the gene of interest, wherein the third base of each codon is changed to an A or a T without changing the corresponding amino acid. In one embodiment, the genes of interest are antibody genes or portions of antibody genes. FIG. 2 shows a schematic drawing of a polynucleotide cassette containing an antibody heavy chain and an antibody light chain as two genes of interest. Antibodies used in or encoded by the polynucleotide cassettes of the present invention include, but are not limited to, IgG, IgM, IgA, IgD, IgE, IgY, lambda chains, kappa chains, bi-specific antibodies, and fragments thereof; scFv fragments, Fc fragments, and Fab fragments as well as dimeric, trimeric and oligomeric forms of antibody fragments. Desired antibodies include, but are not limited to, naturally occurring antibodies, human antibodies, humanized antibodies, autoantibodies and hybrid antibodies. Genes encoding modified versions of naturally occurring antibodies or fragments thereof and genes encoding artificially designed antibodies or fragments thereof may be incorporated into the transposon-based vectors of the present invention. Desired antibodies also include antibodies with the ability to bind specific ligands, for example, antibodies against proteins associated with cancer-related molecules, such as anti-her 2, or anti-CA125. Accordingly, the present invention encompasses a polynucleotide cassette as described herein containing one or more genes encoding a heavy immunoglobulin (Ig) chain and a light Ig chain.

[0083] Antibodies that may be produced using the present invention include, but are not limited to, antibodies for use in cancer immunotherapy against specific antigens, or for providing passive immunity to an animal or a human against an infectious disease or a toxic agent. The antibodies prepared using the methods of the present invention may also be designed to possess specific labels that may be detected through means known to one of ordinary skill in the art. For example, antibodies may be labeled with a fluorescent label attached that may be detected following exposure to specific wavelengths. Such labeled antibodies may be primary antibodies directed to a specific antigen, for example, rhodamine-labeled rabbit anti-growth hormone, or may be labeled secondary antibodies, such as fluorescein-labeled goat-anti chicken IgG. Such labeled antibodies are known to one of ordinary skill in the art. The antibodies may also be designed to possess specific sequences useful for purification through means known to one of ordinary skill in the art. Labels useful for attachment to antibodies are also known to one of ordinary skill in the art. Some of these labels are described in the “Handbook of Fluorescent Probes and Research Products”, ninth edition, Richard P. Haugland (ed) Molecular Probes, Inc. Eugene, Oreg.), which is incorporated herein in its entirety. Antibodies produced with the present invention may be used as laboratory reagents for numerous applications including radioimmunoassay, western blots, dot blots, ELISA, immunoaffinity columns and other procedures requiring antibodies as known to one of ordinary skill in the art. Such antibodies include primary antibodies, secondary antibodies and tertiary antibodies, which may be labeled or unlabeled.

[0084] Additional antibodies that may be made with the practice of the present invention include, but are not limited to, primary antibodies, secondary antibodies, designer antibodies, anti-protein antibodies, anti-peptide antibodies, anti-DNA antibodies, anti-RNA antibodies, anti-hormone antibodies, anti-hypophysiotropic peptides, antibodies against non-natural antigens, anti-anterior pituitary hormone antibodies, anti-posterior pituitary hormone antibodies, anti-venom antibodies, anti-tumor marker antibodies, antibodies directed against epitopes associated with infectious disease, including, anti-viral, anti-bacterial, anti-protozoal, anti-fungal, anti-parasitic, anti-receptor, anti-lipid, anti-phospholipid, anti-growth factor, anti-cytokine, anti-monokine, anti-idiotype, and anti-accessory (presentation) protein antibodies. Antibodies made with the present invention, as well as light chains or heavy chains, may also be used to inhibit enzyme activity.

[0085] Antibodies that may be produced using the present invention include, but are not limited to, antibodies made against the following proteins: Bovine γ-Globulin, Serum; Bovine IgG, Plasma; Chicken γ-Globulin, Serum; Human γ-Globulin, Serum; Human IgA, Plasma; Human IgA₁, Myeloma; Human IgA₂, Myeloma; Human IgA₂, Plasma; Human IgD, Plasma; Human IgE, Myeloma; Human IgG, Plasma; Human IgG, Fab Fragment, Plasma; Human IgG, F(ab′)₂ Fragment, Plasma; Human IgG, Fc Fragment, Plasma; Human IgG₁, Myeloma; Human IgG₂, Myeloma; Human IgG₃, Myeloma; Human IgG₄, Myeloma; Human IgM, Myeloma; Human IgM, Plasma; Human Immunoglobulin, Light Chain κ, Urine; Human Immunoglobulin, Light Chains κ and λ, Plasma; Mouse γ-Globulin, Serum; Mouse IgG, Serum; Mouse IgM, Myeloma; Rabbit γ-Globulin, Serum; Rabbit IgG, Plasma; and Rat γ-Globulin, Serum. In one embodiment, the transposon-based vector comprises the coding sequence of light and heavy chains of a murine monoclonal antibody that shows specificity for human seminoprotein (GenBank Accession numbers AY129006 and AY129304 for the light and heavy chains, respectively).

[0086] A further non-limiting list of antibodies that recognize other antibodies and that may be produced using the present invention is as follows: Anti-Chicken IgG, heavy (H) & light (L) Chain Specific (Sheep); Anti-Goat γ-Globulin (Donkey); Anti-Goat IgG, Fc Fragment Specific (Rabbit); Anti-Guinea Pig γ-Globulin (Goat); Anti-Human Ig, Light Chain, Type κ Specific; Anti-Human Ig, Light Chain, Type λ Specific; Anti-Human IgA, α-Chain Specific (Goat); Anti-Human IgA, Fab Fragment Specific; Anti-Human IgA, Fc Fragment Specific; Anti-Human IgA, Secretory; Anti-Human IgE, ε-Chain Specific (Goat); Anti-Human IgE, Fc Fragment Specific; Anti-Human IgG, Fc Fragment Specific (Goat); Anti-Human IgG, γ-Chain Specific (Goat); Anti-Human IgG, Fc Fragment Specific; Anti-Human IgG, Fd Fragment Specific; Anti-Human IgG, H & L Chain Specific (Goat); Anti-Human IgG₁, Fc Fragment Specific; Anti-Human IgG₂, Fc Fragment Specific; Anti-Human IgG₂, Fd Fragment Specific; Anti-Human IgG₃, Hinge Specific; Anti-Human IgG₄, Fc Fragment Specific; Anti-Human IgM, Fc Fragment Specific; Anti-Human IgM, μ-Chain Specific; Anti-Mouse IgE, ε-Chain Specific; Anti-Mouse γ-Globulin (Goat); Anti-Mouse IgG, γ-Chain Specific (Goat); Anti-Mouse IgG, γ-Chain Specific (Goat) F(ab′)₂ Fragment; Anti-Mouse IgG, H & L Chain Specific (Goat); Anti-Mouse IgM, μ-Chain Specific (Goat); Anti-Mouse IgM, H & L Chain Specific (Goat); Anti-Rabbit γ-Globulin (Goat); Anti-Rabbit IgG, Fc Fragment Specific (Goat); Anti-Rabbit IgG, H & L Chain Specific (Goat); Anti-Rat γ-Globulin (Goat); Anti-Rat IgG, H & L Chain Specific; Anti-Rhesus Monkey γ-Globulin (Goat); and, Anti-Sheep IgG, H & L Chain Specific.

[0087] Antibodies that bind a particular ligand may also be produced. Exemplary ligands are as follows: adrenomedulin, amylin, calcitonin, amyloid, calcitonin gene-related peptide, cholecystokinin, gastrin, gastric inhibitory peptide, gastrin releasing peptide, interleukin, interferon, cortistatin, somatostatin, endothelin, sarafotoxin, glucagon, glucagon-like peptide, insulin, atrial natriuretic peptide, BNP, CNP, neurokinin, substance P, leptin, neuropeptide Y, melanin concentrating hormone, melanocyte stimulating hormone, orphanin, endorphin, dynorphin, enkephalin, enkephalin, leumorphin, peptide F, PACAP, PACAP-related peptide, parathyroid hormone, urocortin, corticotrophin releasing hormone, PHM, PHI, vasoactive intestinal polypeptide, secretin, ACTH, angiotensin, angiostatin, bombesin, endostatin, bradykinin, FMRF amide, galanin, gonadotropin releasing hormone (GnRH) associated peptide, GnRH, growth hormone releasing hormone, inhibin, granulocyte-macrophage colony stimulating factor (GM-CSF), motilin, neurotensin, oxytocin, vasopressin, osteocalcin, pancreastatin, pancreatic polypeptide, peptide YY, proopiomelanocortin, transforming growth factor, vascular endothelial growth factor, vesicular monoamine transporter, vesicular acetylcholine transporter, ghrelin, NPW, NPB, C3d, prokinetican, thyroid stimulating hormone, luteinizing hormone, follicle stimulating hormone, prolactin, growth hormone, beta-lipotropin, melatonin, kallikriens, kinins, prostaglandins, erythropoietin, p146 (SEQ ID NO:78 amino acid sequence, SEQ ID NO:79, nucleotide sequence), estrogen, testosterone, corticosteroids, mineralocorticoids, thyroid hormone, thymic hormones, connective tissue proteins, nuclear proteins, actin, avidin, activin, agrin, albumin, and prohormones, propeptides, splice variants, fragments and analogs thereof.

[0088] The following is yet another non-limiting of antibodies that can be produced by the methods of present invention: abciximab (ReoPro), abciximab anti-platelet aggregation monoclonal antibody, anti-CD11a (hu1124), anti-CD18 antibody, anti-CD20 antibody, anti-cytomegalovirus (CMV) antibody, anti-digoxin antibody, anti-hepatitis B antibody, anti-HER-2 antibody, anti-idiotype antibody to GD3 glycolipid, anti-IgE antibody, anti-IL-2R antibody, antimetastatic cancer antibody (mAb 17-1A), anti-rabies antibody, anti-respiratory syncytial virus (RSV) antibody, anti-Rh antibody, anti-TCR, anti-TNF antibody, anti-VEGF antibody and Fab fragment thereof, rattlesnake venom antibody, black widow spider venom antibody, coral snake venom antibody, antibody against very late antigen-4 (VLA-4), C225 humanized antibody to EGF receptor, chimeric (human & mouse) antibody against TNFα, antibody directed against GPIIb/IIIa receptor on human platelets, gamma globulin, anti-hepatitis B immunoglobulin, human anti-D immunoglobulin, human antibodies against S aureus, human tetanus immunoglobulin, humanized antibody against the epidermal growth receptor-2, humanized antibody against the α subunit of the interleukin-2 receptor, humanized antibody CTLA41G, humanized antibody to the IL-2 R α-chain, humanized anti-CD40-ligand monoclonal antibody (5c8), humanized mAb against the epidermal growth receptor-2, humanized mAb to rous sarcoma virus, humanized recombinant antibody (IgG1k) against respiratory syncytial virus (RSV), lymphocyte immunoglobulin (anti-thymocyte antibody), lymphocyte immunoglobulin, mAb against factor VII, MDX-210 bi-specific antibody against HER-2, MDX-22, MDX-220 bi-specific antibody against TAG-72 on tumors, MDX-33 antibody to FcγR1 receptor, MDX-447 bi-specific antibody against EGF receptor, MDX-447 bispecific humanized antibody to EGF receptor, MDX-RA immunotoxin (ricin A linked) antibody, Medi-507 antibody (humanized form of BTI-322) against CD2 receptor on T-cells, monoclonal antibody LDP-02, muromonab-CD3(OKT3) antibody, OKT3 (“muromomab-CD3”) antibody, PRO542 antibody, ReoPro (“abciximab”) antibody, and TNF-IgG fusion protein.

[0089] Another non-limiting list of the antibodies that may be produced using the present invention is provided in product catalogs of companies such as Phoenix Pharmaceuticals, Inc. (www.phoenixpeptide.com; 530 Harbor Boulevard, Belmont, Calif.), Peninsula Labs San Carlos Calif., SIGMA, St. Louis, Mo. www.sigma-aldrich.com, Cappel ICN, Irvine, Calif., www.icnbiomed.com, and Calbiochem, La Jolla, Calif., www.calbiochem.com, which are all incorporated herein by reference in their entirety. The polynucleotide sequences encoding these antibodies may be obtained from the scientific literature, from patents, and from databases such as GenBank. Alternatively, one of ordinary skill in the art may design the antibody polynucleotide sequence by choosing the codons that encode for each amino acid in the desired antibody.

[0090] Genes encoding protein and peptide hormones are a preferred class of genes of interest in the present invention. Such protein and peptide hormones are synthesized throughout the endocrine system and include, but are not limited to, hypothalamic hormones and hypophysiotropic hormones, anterior, intermediate and posterior pituitary hormones, pancreatic islet hormones, hormones made in the gastrointestinal system, renal hormones, thymic hormones, parathyroid hormones, adrenal cortical and medullary hormones. Specifically, hormones that can be produced using the present invention include, but are not limited to, chorionic gonadotropin, corticotropin, erythropoietin, glucagons, IGF-1, oxytocin, platelet-derived growth factor, calcitonin, follicle-stimulating hormone, luteinizing hormone, thyroid-stimulating hormone, insulin, gonadotropin-releasing hormone and its analogs, vasopressin, octreotide, somatostatin, prolactin, adrenocorticotropic hormone, antidiuretic hormone, thyrotropin-releasing hormone (TRH), growth hormone-releasing hormone (GHRH), dopamine, melatonin, thyroxin (T₄), parathyroid hormone (PTH), glucocorticoids such as cortisol, mineralocorticoids such as aldosterone, androgens such as testosterone, adrenaline (epinephrine), noradrenaline (norepinephrine), estrogens such as estradiol, progesterone, glucagons, calcitrol, calciferol, atrial-natriuretic peptide, gastrin, secretin, cholecystokinin (CCK), neuropeptide Y, ghrelin, PYY₃₋₃₆, angiotensinogen, thrombopoietin, and leptin. By using appropriate polynucleotide sequences, species-specific hormones may be made by transgenic animals.

[0091] In one embodiment of the present invention, the gene of interest is a proinsulin gene and the desired molecule is insulin. Proinsulin consists of three parts: a C-peptide and two strands of amino acids (the alpha and beta chains) that later become linked together to form the insulin molecule. In these embodiments, proinsulin is expressed in the oviduct tubular gland cells and then deposited in the egg white. One example of a proinsulin polynucleotide sequence is shown in SEQ ID NO:80, wherein the C-peptide cleavage site spans from Arg at position 31 to Arg at position 65.

[0092] Further included in the present invention are genes of interet that encode proteins and peptides synthesized by the immune system including those synthesized by the thymus, lymph nodes, spleen, and the gastrointestinal associated lymph tissues (GALT) system. The immune system proteins and peptides proteins that can be made in transgenic animals using the polynucleotide cassettes of the present invention include, but are not limited to, alpha-interferon, beta-interferon, gamma-interferon, alpha-interferon A, alpha-interferon 1, G-CSF, GM-CSF, interlukin-1 (IL-1), IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, TNF-α, and TNF-β. Other cytokines included in the present invention include cardiotrophin, stromal cell derived factor, macrophage derived chemokine (MDC), melanoma growth stimulatory activity (MGSA), macrophage inflammatory proteins 1 alpha (MIP-1 alpha), 2, 3 alpha, 3 beta, 4 and 5.

[0093] Genes encoding lytic peptides such as p146 are also included in the genes of interest of the present invention. In one embodiment, the p146 peptide comprises an amino acid sequence of SEQ ID NO:78. The present invention also encompasses a polynucleotide cassette comprising a p146 nucleic acid having a sequence of SEQ ID NO:79.

[0094] Enzymes are another class of proteins that may be encoded by the polynucleotide cassettes of the present invention. Such enzymes include but are not limited to adenosine deaminase, alpha-galactosidase, cellulase, collagenase, dnasel, hyaluronidase, lactase, L-asparaginase, pancreatin, papain, streptokinase B, subtilisin, superoxide dismutase, thrombin, trypsin, urokinase, fibrinolysin, glucocerebrosidase and plasminogen activator. In some embodiments wherein the enzyme could have deleterious effects, additional amino acids and a protease cleavage site are added to the carboxy end of the enzyme of interest in order to prevent expression of a functional enzyme. Subsequent digestion of the enzyme with a protease results in activation of the enzyme.

[0095] Extracellular matrix proteins are one class of desired proteins that may be encoded by the polynucleotide cassettes of the present invention. Examples include but are not limited to collagen, fibrin, elastin, laminin, and fibronectin and subtypes thereof. Intracellular proteins and structural proteins are other classes of desired proteins in the present invention.

[0096] Growth factors are another desired class of proteins that may be encoded by the polynucleotide cassettes of the present invention and include, but are not limited to, transforming growth factor-α (“TGF-α”), transforming growth factor-β (TGF-β), platelet-derived growth factors (PDGF), fibroblast growth factors (FGF), including FGF acidic isoforms 1 and 2, FGF basic form 2 and FGF 4, 8, 9 and 10, nerve growth factors (NGF) including NGF 2.5s, NGF 7.0s and beta NGF and neurotrophins, brain derived neurotrophic factor, cartilage derived factor, growth factors for stimulation of the production of red blood cells, growth factors for stimulation of the production of white blood cells, bone growth factors (BGF), basic fibroblast growth factor, vascular endothelial growth factor (VEGF), granulocyte colony stimulating factor (G-CSF), insulin like growth factor (IGF) I and II, hepatocyte growth factor, glial neurotrophic growth factor (GDNF), stem cell factor (SCF), keratinocyte growth factor (KGF), transforming growth factors (TGF), including TGFs alpha, beta, beta1, beta2, beta3, skeletal growth factor, bone matrix derived growth factors, bone derived growth factors, erythropoietin (EPO) and mixtures thereof.

[0097] Another desired class of proteins that may be encoded by the polynucleotide cassettes of the present invention include, but are not limited to, leptin, leukemia inhibitory factor (LIF), tumor necrosis factor alpha and beta, ENBREL, angiostatin, endostatin, thrombospondin, osteogenic protein-1, bone morphogenetic proteins 2 and 7, osteonectin, somatomedin-like peptide, and osteocalcin.

[0098] Yet another desired class of proteins encoded by the genes of interet are blood proteins or clotting cascade protein including albumin, Prekallikrein, High molecular weight kininogen (HMWK) (contact activation cofactor; Fitzgerald, Flaujeac Williams factor), Factor I (Fibrinogen), Factor II (prothrombin), Factor III (Tissue Factor), Factor IV (calcium), Factor V (proaccelerin, labile factor, accelerator (Ac-) globulin), Factor VI (Va) (accelerin), Factor VII (proconvertin), serum prothrombin conversion accelerator (SPCA), cothromboplastin), Factor VIII (antihemophiliac factor A, antihemophilic globulin (AHG)), Factor IX (Christmas Factor, antihemophilic factor B, plasma thromboplastin component (PTC)), Factor X (Stuart-Prower Factor), Factor XI (Plasma thromboplastin antecedent (PTA)), Factor XII (Hageman Factor), Factor XIII (rotransglutaminase, fibrin stabilizing factor (FSF), fibrinoligase), von Willebrand factor, Protein C, Protein S, Thrombomodulin, Antithrombin III.

[0099] A non-limiting list of the peptides and proteins that may be encoded by the polynucleotide cassettes of the present invention is provided in product catalogs of companies such as Phoenix Pharmaceuticals, Inc. (www.phoenixpeptide.com; 530 Harbor Boulevard, Belmont, Calif.), Peninsula Labs (San Carlos Calif.), SIGMA, (St. Louis, Mo. www.sigma-aldrich.com), Cappel ICN (Irvine, Calif., www.icnbiomed.com), and Calbiochem (La Jolla, Calif., www.calbiochem.com). The polynucleotide sequences encoding these proteins and peptides of interest may be obtained from the scientific literature, from patents, and from databases such as GenBank. Alternatively, one of ordinary skill in the art may design the polynucleotide sequence to be incorporated into the genome by choosing the codons that encode for each amino acid in the desired protein or peptide.

[0100] Some of these desired proteins or peptides that may be encoded by the polynucleotide cassettes of the present invention include but are not limited to the following: adrenomedulin, amylin, calcitonin, amyloid, calcitonin gene-related peptide, cholecystokinin, gastrin, gastric inhibitory peptide, gastrin releasing peptide, interleukin, interferon, cortistatin, somatostatin, endothelin, sarafotoxin, glucagon, glucagon-like peptide, insulin, atrial natriuretic peptide, BNP, CNP, neurokinin, substance P, leptin, neuropeptide Y, melanin concentrating hormone, melanocyte stimulating hormone, orphanin, endorphin, dynorphin, enkephalin, leumorphin, peptide F, PACAP, PACAP-related peptide, parathyroid hormone, urocortin, corticotrophin releasing hormone, PHM, PHI, vasoactive intestinal polypeptide, secretin, ACTH, angiotensin, angiostatin, bombesin, endostatin, bradykinin, FMRF amide, galanin, gonadotropin releasing hormone (GnRH) associated peptide, GnRH, growth hormone releasing hormone, inhibin, granulocyte-macrophage colony stimulating factor (GM-CSF), motilin, neurotensin, oxytocin, vasopressin, osteocalcin, pancreastatin, pancreatic polypeptide, peptide YY, proopiomelanocortin, transforming growth factor, vascular endothelial growth factor, vesicular monoamine transporter, vesicular acetylcholine transporter, ghrelin, NPW, NPB, C3d, prokinetican, thyroid stimulating hormone, luteinizing hormone, follicle stimulating hormone, prolactin, growth hormone, beta-lipotropin, melatonin, kallikriens, kinins, prostaglandins, erythropoietin, p146 (SEQ ID NO:78, amino acid sequence, SEQ ID NO:79, nucleotide sequence), thymic hormones, connective tissue proteins, nuclear proteins, actin, avidin, activin, agrin, albumin, apolipoproteins, apolipoprotein A, apolipoprotein B, and prohormones, propeptides, splice variants, fragments and analogs thereof.

[0101] Other desired proteins that may be encoded by the polynucleotide cassettes of the present invention include bacitracin, polymixin b, vancomycin, cyclosporine, anti-RSV antibody, alpha-1 antitrypsin (AAT), anti-cytomegalovirus antibody, anti-hepatitis antibody, anti-inhibitor coagulant complex, anti-rabies antibody, anti-Rh(D) antibody, adenosine deaminase, anti-digoxin antibody, antivenin crotalidae (rattlesnake venom antibody), antivenin latrodectus (black widow spider venom antibody), antivenin micrurus (coral snake venom antibody), aprotinin, corticotropin (ACTH), diphtheria antitoxin, lymphocyte immune globulin (anti-thymocyte antibody), protamine, thyrotropin, capreomycin, α-galactosidase, gramicidin, streptokinase, tetanus toxoid, tyrothricin, IGF-1, proteins of varicella vaccine, anti-TNF antibody, anti-IL-2r antibody, anti-HER-2 antibody, OKT3 (“muromonab-CD3”) antibody, TNF-IgG fusion protein, ReoPro (“abciximab”) antibody, ACTH fragment 1-24, desmopressin, gonadotropin-releasing hormone, histrelin, leuprolide, lypressin, nafarelin, peptide that binds GPIIb/GPIIIa on platelets (integrilin), goserelin, capreomycin, colistin, anti-respiratory syncytial virus, lymphocyte immune globulin (Thymoglovin, Atgam), panorex, alpha-antitrypsin, botulinin, lung surfactant protein, tumor necrosis receptor-IgG fusion protein (enbrel), gonadorelin, proteins of influenza vaccine, proteins of rotavirus vaccine, proteins of haemophilus b conjugate vaccine, proteins of poliovirus vaccine, proteins of pneumococcal conjugate vaccine, proteins of meningococcal C vaccine, proteins of influenza vaccine, megakaryocyte growth and development factor (MGDF), neuroimmunophilin ligand-A (NIL-A), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), leptin (native), leptin B, leptin C, IL-IRA (interleukin-IRA), R-568, novel erythropoiesis-stimulating protein (NESP), humanized mAb to rous sarcoma virus (MEDI-493), glutamyl-tryptophan dipeptide IM862, LFA-3TIP immunosuppressive, humanized anti-CD40-ligand monoclonal antibody (5c8), gelsonin enzyme, tissue factor pathway inhibitor (TFPI), proteins of meningitis B vaccine, antimetastatic cancer antibody (mAb 17-1A), chimeric (human & mouse) mAb against TNFα, mAb against factor VII, relaxin, capreomycin, glycopeptide (LY333328), recombinant human activated protein C (rhAPC), humanized mAb against the epidermal growth receptor-2, altepase, anti-CD20 antigen, C2B8 antibody, insulin-like growth factor-1, atrial natriuretic peptide (anaritide), tenectaplase, anti-CD11a antibody (hu 1124), anti-CD18 antibody, mAb LDP-02, anti-VEGF antibody, Fab fragment of anti-VEGF Ab, APO2 ligand (tumor necrosis factor-related apoptosis-inducing ligand), rTGF-β (transforming growth factor-β), alpha-antitrypsin, ananain (a pineapple enzyme), humanized mAb CTLA41G, PRO542 (mAb), D2E7 (mAb), calf intestine alkaline phosphatase, α-L-iduronidase, α-L-galactosidase (humanglutamic acid decarboxylase, acid sphingomyelinase, bone morphogenetic protein-2 (rhBMP-2), proteins of HIV vaccine, T cell receptor (TCR) peptide vaccine, TCR peptides, V beta 3 and V beta 13.1. (IR502), (IR501), BI 1050/1272 mAb against very late antigen-4 (VLA-4), C225 humanized mAb to EGF receptor, anti-idiotype antibody to GD3 glycolipid, antibacterial peptide against H. pylori, MDX-447 bispecific humanized mAb to EGF receptor, anti-cytomegalovirus (CMV), Medi-491 B19 parvovirus vaccine, humanized recombinant mAb (IgG1k) against respiratory syncytial virus (RSV), urinary tract infection vaccine (against “pili” on Escherechia coli strains), proteins of lyme disease vaccine against B. burgdorferi protein (DbpA), proteins of Medi-501 human papilloma virus-11 vaccine (HPV), Streptococcus pneumoniae vaccine, Medi-507 mAb (humanized form of BTI-322) against CD2 receptor on T-cells, MDX-33 mAb to FcγR1 receptor, MDX-RA immunotoxin (ricin A linked) mAb, MDX-210 bi-specific mAb against HER-2, MDX-447 bi-specific mAb against EGF receptor, MDX-22, MDX-220 bi-specific mAb against TAG-72 on tumors, colony-stimulating factor (CSF) (molgramostim), humanized mAb to the IL-2 R α-chain (basiliximab), mAb to IgE (IGE 025A), myelin basic protein-altered peptide (MSP771A), humanized mAb against the epidermal growth receptor-2, humanized mAb against the α subunit of the interleukin-2 receptor, low molecular weight heparin, anti-hemophillic factor, and bactericidal/permeability-increasing protein (r-BPI).

[0102] Other multimeric proteins that may be produced using the present invention are as follows: factors involved in the synthesis or replication of DNA, such as DNA polymerase alpha and DNA polymerase delta; proteins involved in the production of mRNA, such as TFIID and TFIIH; cell, nuclear and other membrane-associated proteins, such as hormone and other signal transduction receptors, active transport proteins and ion channels, multimeric proteins in the blood, including hemoglobin, fibrinogen and von Willabrand's Factor; proteins that form structures within the cell, such as actin, myosin, and tubulin and other cytoskeletal proteins; proteins that form structures in the extra cellular environment, such as collagen, elastin and fibronectin; proteins involved in intra- and extra-cellular transport, such as kinesin and dynein, the SNARE family of proteins (soluble NSF attachment protein receptor) and clathrin; proteins that help regulate chromatin structure, such as histones and protamines, Swi3p, Rsc8p and moira; multimeric transcription factors such as Fos, Jun and CBTF (CCAAT box transcription factor); multimeric enzymes such as acetylcholinesterase and alcohol dehydrogenase; chaperone proteins such as GroE, Gro EL (chaperonin 60) and Gro ES(chaperonin 10); anti-toxins, such as snake venom, botulism toxin, Streptococcus super antigens; lysins (enzymes from bacteriophage and viruses); as well as most allosteric proteins.

[0103] The multimeric proteins made using the present invention may be labeled using labels and techniques known to one of ordinary skill in the art. Some of these labels are described in the “Handbook of Fluorescent Probes and Research Products”, ninth edition, Richard P. Haugland (ed) Molecular Probes, Inc. Eugene, Oreg.), which is incorporated herein in its entirety. Some of these labels may be genetically engineered into the polynucleotide sequence for the expression of the selected multimeric protein. The peptides and proteins may also have label-incorporation “handles” incorporated to allow labeling of an otherwise difficult or impossible to label multimeric protein.

[0104] It is to be understood that the various classes of desired peptides and proteins, as well as specific peptides and proteins described in this section may be modified as described below by inserting selected codons for desired amino acid substitutions into the gene incorporated into the transgenic animal.

[0105] The present invention may also be used to produce desired molecules other than proteins and peptides including, but not limited to, lipoproteins such as high density lipoprotein (HDL), HDL-Milano, and low density lipoprotein, lipids, carbohydrates, siRNA and ribozymes. In these embodiments, a gene of interest encodes a nucleic acid molecule or a protein that directs production of the desired molecule.

[0106] The present invention further encompasses the use of inhibitory molecules to inhibit endogenous (i.e., non-vector) protein production. These inhibitory molecules include antisense nucleic acids, siRNA and inhibitory proteins. In a preferred embodiment, the endogenous protein whose expression is inhibited is an egg white protein including, but not limited to ovalbumin, ovotransferrin, and ovomucin ovomucoid, ovoinhibitor, cystatin, ovostatin, lysozyme, ovoglobulin G2, ovoglobulin G3, avidin, and thiamin binding protein. In one embodiment, a polynucleotide cassette containing an ovalbumin DNA sequence, that upon transcription forms a double stranded RNA molecule, is transfected into an animal such as a bird and the bird's production of endogenous ovalbumin protein is reduced by the interference RNA mechanism (RNAi). In other embodiments, a polynucleotide cassette encodes an inhibitory RNA molecule that inhibits the expression of more than one egg white protein. Additionally, inducible knockouts or knockdowns of the endogenous protein may be created to achieve a reduction or inhibition of endogenous protein production. Endogenous egg white production can be inhibited in an avian at any time, but is preferably inhibited preceding, or immediately preceding, the harvest of eggs.

[0107] Modified Desired Proteins and Peptides

[0108] The present invention may be used for the production of multimeric proteins. “Proteins”, “peptides,” “polypeptides” and “oligopeptides” are chains of amino acids (typically L-amino acids) whose alpha carbons are linked through peptide bonds formed by a condensation reaction between the carboxyl group of the alpha carbon of one amino acid and the amino group of the alpha carbon of another amino acid. The terminal amino acid at one end of the chain (i.e., the amino terminal) has a free amino group, while the terminal amino acid at the other end of the chain (i.e., the carboxy terminal) has a free carboxyl group. As such, the term “amino terminus” (abbreviated N-terminus) refers to the free alpha-amino group on the amino acid at the amino terminal of the protein, or to the alpha-amino group (imino group when participating in a peptide bond) of an amino acid at any other location within the protein. Similarly, the term “carboxy terminus” (abbreviated C-terminus) refers to the free carboxyl group on the amino acid at the carboxy terminus of a protein, or to the carboxyl group of an amino acid at any other location within the protein.

[0109] Typically, the amino acids making up a protein are numbered in order, starting at the amino terminal and increasing in the direction toward the carboxy terminal of the protein. Thus, when one amino acid is said to “follow” another, that amino acid is positioned closer to the carboxy terminal of the protein than the preceding amino acid.

[0110] The term “residue” is used herein to refer to an amino acid (D or L) or an amino acid mimetic that is incorporated into a protein by an amide bond. As such, the amino acid may be a naturally occurring amino acid or, unless otherwise limited, may encompass known analogs of natural amino acids that function in a manner similar to the naturally occurring amino acids (i.e., amino acid mimetics). Moreover, an amide bond mimetic includes peptide backbone modifications well known to those skilled in the art.

[0111] Furthermore, one of skill will recognize that, as mentioned above, individual substitutions, deletions or additions which alter, add or delete a single amino acid or a small percentage of amino acids (typically less than about 5%, more typically less than about 1%) in an encoded sequence are conservatively modified variations where the alterations result in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables providing functionally similar amino acids are well known in the art. The following six groups each contain amino acids that are conservative substitutions for one another:

[0112] 1) Alanine (A), Serine (S), Threonine (T);

[0113] 2) Aspartic acid (D), Glutamic acid (E);

[0114] 3) Asparagine (N), Glutamine (Q);

[0115] 4) Arginine (R), Lysine (K);

[0116] 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); and

[0117] 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W).

[0118] A conservative substitution is a substitution in which the substituting amino acid (naturally occurring or modified) is structurally related to the amino acid being substituted, i.e., has about the same size and electronic properties as the amino acid being substituted. Thus, the substituting amino acid would have the same or a similar functional group in the side chain as the original amino acid. A “conservative substitution” also refers to utilizing a substituting amino acid which is identical to the amino acid being substituted except that a functional group in the side chain is protected with a suitable protecting group.

[0119] Suitable protecting groups are described in Green and Wuts, “Protecting Groups in Organic Synthesis”, John Wiley and Sons, Chapters 5 and 7, 1991, the teachings of which are incorporated herein by reference. Preferred protecting groups are those which facilitate transport of the peptide through membranes, for example, by reducing the hydrophilicity and increasing the lipophilicity of the peptide, and which can be cleaved, either by hydrolysis or enzymatically (Ditter et al., 1968. J. Pharm. Sci. 57:783; Ditter et al., 1968. J. Pharm. Sci. 57:828; Ditter et al., 1969. J. Pharm. Sci. 58:557; King et al., 1987. Biochemistry 26:2294; Lindberg et al., 1989. Drug Metabolism and Disposition 17:311; Tunek et al., 1988. Biochem. Pharm. 37:3867; Anderson et al., 1985 Arch. Biochem. Biophys. 239:538; and Singhal et al., 1987. FASEB J. 1:220). Suitable hydroxyl protecting groups include ester, carbonate and carbamate protecting groups. Suitable amine protecting groups include acyl groups and alkoxy or aryloxy carbonyl groups, as described above for N-terminal protecting groups. Suitable carboxylic acid protecting groups include aliphatic, benzyl and aryl esters, as described below for C-terminal protecting groups. In one embodiment, the carboxylic acid group in the side chain of one or more glutamic acid or aspartic acid residues in a peptide of the present invention is protected, preferably as a methyl, ethyl, benzyl or substituted benzyl ester, more preferably as a benzyl ester.

[0120] Provided below are groups of naturally occurring and modified amino acids in which each amino acid in a group has similar electronic and steric properties. Thus, a conservative substitution can be made by substituting an amino acid with another amino acid from the same group. It is to be understood that these groups are non-limiting, i.e. that there are additional modified amino acids which could be included in each group.

[0121] Group I includes leucine, isoleucine, valine, methionine and modified amino acids having the following side chains: ethyl, n-propyl n-butyl. Preferably, Group I includes leucine, isoleucine, valine and methionine.

[0122] Group II includes glycine, alanine, valine and a modified amino acid having an ethyl side chain. Preferably, Group II includes glycine and alanine.

[0123] Group III includes phenylalanine, phenylglycine, tyrosine, tryptophan, cyclohexylmethyl glycine, and modified amino residues having substituted benzyl or phenyl side chains. Preferred substituents include one or more of the following: halogen, methyl, ethyl, nitro, —NH₂, methoxy, ethoxy and —CN. Preferably, Group III includes phenylalanine, tyrosine and tryptophan.

[0124] Group IV includes glutamic acid, aspartic acid, a substituted or unsubstituted aliphatic, aromatic or benzylic ester of glutamic or aspartic acid (e.g., methyl, ethyl, n-propyl iso-propyl, cyclohexyl, benzyl or substituted benzyl), glutamine, asparagine, O—NH— alkylated glutamine or asparagines (e.g., methyl, ethyl, n-propyl and iso-propyl) and modified amino acids having the side chain —(CH₂)₃—OOH, an ester thereof (substituted or unsubstituted aliphatic, aromatic or benzylic ester), an amide thereof and a substituted or unsubstituted N-alkylated amide thereof. Preferably, Group IV includes glutamic acid, aspartic acid, methyl aspartate, ethyl aspartate, benzyl aspartate and methyl glutamate, ethyl glutamate and benzyl glutamate, glutamine and asparagine.

[0125] Group V includes histidine, lysine, omithine, arginine, N-nitroarginine, β-cycloarginine, γ-hydroxyarginine, N-amidinocitruline and 2-amino-4-guanidinobutanoic acid, homologs of lysine, homologs of arginine and homologs of omithine. Preferably, Group V includes histidine, lysine, arginine and ornithine. A homolog of an amino acid includes from 1 to about 3 additional or subtracted methylene units in the side chain.

[0126] Group VI includes serine, threonine, cysteine and modified amino acids having C1-C5 straight or branched alkyl side chains substituted with —OH or —SH, for example, CH₂CH₂OH, CH₂CH₂CH₂OH or —CH₂CH₂OHCH₃. Preferably, Group VI includes serine, cysteine or threonine.

[0127] In another aspect, suitable substitutions for amino acid residues include “severe” substitutions. A “severe substitution” is a substitution in which the substituting amino acid (naturally occurring or modified) has significantly different size and/or electronic properties compared with the amino acid being substituted. Thus, the side chain of the substituting amino acid can be significantly larger (or smaller) than the side chain of the amino acid being substituted and/or can have functional groups with significantly different electronic properties than the amino acid being substituted. Examples of severe substitutions of this type include the substitution of phenylalanine or cyclohexylmethyl glycine for alanine, isoleucine for glycine, a D amino acid for the corresponding L amino acid, or —NH—CH[(—CH₂)₅—COOH]—CO— for aspartic acid. Alternatively, a functional group may be added to the side chain, deleted from the side chain or exchanged with another functional group. Examples of severe substitutions of this type include adding of valine, leucine or isoleucine, exchanging the carboxylic acid in the side chain of aspartic acid or glutamic acid with an amine, or deleting the amine group in the side chain of lysine or omithine. In yet another alternative, the side chain of the substituting amino acid can have significantly different steric and electronic properties that the functional group of the amino acid being substituted. Examples of such modifications include tryptophan for glycine, lysine for aspartic acid and —(CH₂)₄COOH for the side chain of serine. These examples are not meant to be limiting.

[0128] In another embodiment, for example in the synthesis of a peptide 26 amino acids in length, the individual amino acids may be substituted according in the following manner:

[0129] AA₁ is serine, glycine, alanine, cysteine or threonine;

[0130] AA₂ is alanine, threonine, glycine, cysteine or serine;

[0131] AA₃ is valine, arginine, leucine, isoleucine, methionine, omithine, lysine, N-nitroarginine, β-cycloarginine, γ-hydroxyarginine, N-amidinocitruline or 2-amino-4-guanidinobutanoic acid;

[0132] AA₄ is proline, leucine, valine, isoleucine or methionine;

[0133] AA₅ is tryptophan, alanine, phenylalanine, tyrosine or glycine;

[0134] AA₆ is serine, glycine, alanine, cysteine or threonine;

[0135] AA₇ is proline, leucine, valine, isoleucine or methionine;

[0136] AA₈ is alanine, threonine, glycine, cysteine or serine;

[0137] AA₉ is alanine, threonine, glycine, cysteine or serine;

[0138] AA₁₀ is leucine, isoleucine, methionine or valine;

[0139] AA₁₁ is serine, glycine, alanine, cysteine or threonine;

[0140] AA₁₂ is leucine, isoleucine, methionine or valine;

[0141] AA₁₃ is leucine, isoleucine, methionine or valine;

[0142] AA₁₄ is glutamine, glutamic acid, aspartic acid, asparagine, or a substituted or unsubstituted aliphatic or aryl ester of glutamic acid or aspartic acid;

[0143] AA₁₅ is arginine, N-nitroarginine, β-cycloarginine, γ-hydroxy-arginine, N-amidinocitruline or 2-amino-4-guanidino-butanoic acid

[0144] AA₁₆ is proline, leucine, valine, isoleucine or methionine;

[0145] AA₁₇ is serine, glycine, alanine, cysteine or threonine;

[0146] AA₁₈ is glutamic acid, aspartic acid, asparagine, glutamine or a substituted or unsubstituted aliphatic or aryl ester of glutamic acid or aspartic acid;

[0147] AA₁₉ is aspartic acid, asparagine, glutamic acid, glutamine, leucine, valine, isoleucine, methionine or a substituted or unsubstituted aliphatic or aryl ester of glutamic acid or aspartic acid;

[0148] AA₂₀ is valine, arginine, leucine, isoleucine, methionine, ornithine, lysine, N-nitroarginine, β-cycloarginine, γ-hydroxyarginine, N-amidinocitruline or 2-amino-4-guanidinobutanoic acid;

[0149] AA₂₁ is alanine, threonine, glycine, cysteine or serine;

[0150] AA₂₂ is alanine, threonine, glycine, cysteine or serine;

[0151] AA₂₃ is histidine, serine, threonine, cysteirie, lysine or ornithine;

[0152] AA₂₄ is threonine, aspartic acid, serine, glutamic acid or a substituted or unsubstituted aliphatic or aryl ester of glutamic acid or aspartic acid;

[0153] AA₂₅ is asparagine, aspartic acid, glutamic acid, glutamine, leucine, valine, isoleucine, methionine or a substituted or unsubstituted aliphatic or aryl ester of glutamic acid or aspartic acid; and

[0154] AA₂₆ is cysteine, hisfidine, serine, threonine, lysine or ornithine.

[0155] It is to be understood that these amino acid substitutions may be made for longer or shorter peptides than the 26 mer in the preceding example above, and for proteins.

[0156] In one embodiment of the present invention, codons for the first several N-terminal amino acids of the transposase are modified such that the third base of each codon is changed to an A or a T without changing the corresponding amino acid. It is preferable that between approximately 1 and 20, more preferably 3 and 15, and most preferably between 4 and 12 of the first N-terminal codons of the gene of interest are modified such that the third base of each codon is changed to an A or a T without changing the corresponding amino acid. In one embodiment, the first ten N-terminal codons of the gene of interest are modified in this manner.

[0157] When several desired proteins, protein fragments or peptides are encoded in the gene of interest to be incorporated into the genome, as with the multivalent multimeric proteins, one of skill in the art will appreciate that the proteins, protein fragments or peptides may be separated by a spacer molecule such as, for example, a peptide, consisting of one or more amino acids. Generally, the spacer will have no specific biological activity other than to join the desired proteins, protein fragments or peptides together, or to preserve some minimum distance or other spatial relationship between them. However, the constituent amino acids of the spacer may be selected to influence some property of the molecule such as the folding, net charge, or hydrophobicity. The spacer may also be contained within a nucleotide sequence with a purification handle or be flanked by proteolytic cleavage sites.

[0158] Such polypeptide spacers may have from about 1 to about 100 amino acids, preferably 3 to 20 amino acids, and more preferably 4-15 amino acids. The spacers in a polypeptide are independently chosen, but are preferably all the same. The spacers should allow for flexibility of movement in space and are therefore typically rich in small amino acids, for example, glycine, serine, proline or alanine. Preferably, peptide spacers contain at least 60%, more preferably at least 80% glycine or alanine. In addition, peptide spacers generally have little or no biological and antigenic activity. Preferred spacers are (Gly-Pro-Gly-Gly)_(x) (SEQ ID NO:81) and (Gly₄-Ser)_(y), wherein x is an integer from about 3 to about 9 and y is an integer from about 1 to about 8. Specific examples of suitable spacers include (Gly-Pro-Gly-Gly)₃ Gly Pro Gly Gly Gly Pro Gly Gly Gly SEQ ID NO: 82 Pro Gly Gly (Gly₄-Ser)₃ Gly Gly Gly Gly Ser Gly Gly Gly Gly SEQ ID NO: 83 Ser Gly Gly Gly Gly Ser or (Gly₄-Ser)₄ Gly Gly Gly Gly Ser Gly Gly Gly Gly SEQ ID NO: 84 Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser.

[0159] One example of a multivalent multimeric protein containin a spacer is leutinizing hormone (LH), normally made as separate alpha and beta chains, made as a single polypeptide as described in Galet et. al., Mol. Cell Endocrinology, 2001, 174 (1-2):31-40. Production of a multimeric protein may thus be simplified using a spacer sequence that may or may not contain cleavage sites. In the case of an immunoglobulin, for example, a heavy and light chain may be synthesized as a single polypeptide using a spacer sequence with protease sites native to the transgenic animal so as to make, upon processing, a heavy and light chain combination in close association, facilitating the addition of a similar heavy and light chain to produce the native immunoglobulin. In this model, the removal of the spacer sequence may or may not be required. Other multimeric proteins may be made in bioengineered organisms in a similar fashion.

[0160] Nucleotide sequences encoding for the production of residues which may be useful in purification of the expressed recombinant protein may also be built into the vector. Such sequences are known in the art and include the glutathione binding domain from glutathione S-transferase, polylysine, hexa-histidine or other cationic amino acids, thioredoxin, hemagglutinin antigen and maltose binding protein.

[0161] Additionally, nucleotide sequences may be inserted into the gene of interest to be incorporated so that the protein or peptide can also include from one to about six amino acids that create signals for proteolytic cleavage. In this manner, if a gene is designed to make one or more peptides or proteins of interest in the transgenic animal, specific nucleotide sequences encoding for amino acids recognized by enzymes may be incorporated into the gene to facilitate cleavage of the large protein or peptide sequence into desired peptides or proteins or both. For example, nucleotides encoding a proteolytic cleavage site can be introduced into the gene of interest so that a signal sequence can be cleaved from a protein or peptide encoded by the gene of interest. Nucleotide sequences encoding other amino acid sequences which display pH sensitivity, chemical sensitivity or photolability may also be added to the vector to facilitate separation of the signal sequence from the peptide or protein of interest.

[0162] Proteolytic cleavage sites include cleavage sites recognized by exopeptidases such as carboxypeptidase A, carboxypeptidase B, aminopeptidase I, and dipeptidylaminopeptidase; endopeptidases such as trypsin, V8-protease, enterokinase, factor Xa, collagenase, endoproteinase, subtilisin, and thombin; and proteases such as Protease 3C IgA protease (Igase) Rhinovirus 3C(preScission)protease. Chemical cleavage sites are also included in the defintion of cleavage site as used herein. Chemical cleavage sites include, but are not limited to, site cleaved by cyanogen bromide, hydroxylamine, formic acid, and acetic acid. Self-splicing cleavage sites such as inteins are also included in the present invention.

[0163] In some embodiments, one or more cleavage sites are incorporated into a polynucleotide cassette containing multiple genes of interest. FIG. 4 depicts one example of a polynucleotide cassette containing two genes of interest containing a cleavage site between them. The genes of interest may encode different proteins or peptides, the same protein or peptide, or modified versions of the same protein or peptide. While FIG. 4 shows a polynucleotide cassette containing two genes of interest, the present invention encompasses a polynucleotide cassette containing any number of genes of interest. The cleavage site located between the genes of interest can encode any amino acid sequence that is cleaved by any means. As mentioned above, the cleavage site can encode an amino acid sequence cleaved by a protease, a chemical reaction, can be a photolabile site, or can be a pro polynucleotide

[0164] The present invention includes a polynucleotide cassette that encodes a repetitive polypeptide chain in which two or more peptides, polypeptides or proteins, designated as P in the structural formulae presented below, are each separated by a peptide spacer or cleavage site designated as B. A polypeptide multivalent ligand, also called a multivalent protein, is a form of a multimeric protein encoded by the polynucleotide cassettes of the present invention, and is represented by structural formulae (I, II and III). Each peptide or protein is connected to another peptide or protein through a peptide bond, to a linker group, to a spacer, or to a cleavage site. Each peptide, polypeptide or protein may be the same or different and each linker, spacer, cleavage site or covalent bond is independently chosen.

[0165] A “polypeptide multivalent protein” is a multiple repeat polypeptide chain in which two or more peptides P are each separated by a peptide linker group, a spacer or a cleavage site. A polypeptide multivalent ligand is represented by structural formulae II and III.

B-(L-P)n  I

[0166] wherein B is a peptide spacer or cleavage site, n is an integer from 2 to about 20, each L is a covalent bond, a linking group or cleavage site which may be present or absent, and each P is a peptide having from about 4 to about 200 amino acid residues.

P—(B—P)m-B—P  II

[0167] wherein m is an integer from 0 to about 20.

Pa—(B)n-Pa  III

[0168] wherein n is an integer from 1 to 20, preferably 2 to 10, more preferably 3 to 7, further wherein a is 1.

[0169] Other examples of multivalent proteins include the following:

P_(y)-L_(x)-B_(n)-L_(x)-Py  IV

P_(y)—B—P_(y)

[0170] In the preceding structural formulae IV and V of polypeptide multivalent ligands encoded by a polynucleotide cassette of the present invention, each P is a peptide having from about 4 to about 200 amino acid residues, y is 1, x is an integer from 1 to 3, and n is an integer from 1 to 20, preferably 2 to 10, more preferably 3 to 7. Each B is a peptide spacer or cleavage site comprised of at least 2 amino acids or a cleavage site. Each peptide P and each B are independently chosen and may be the same or different.

[0171] Suitable linkers (L) are groups that can connect peptides and proteins to each other. In one example, the linker is an oligopeptide of from about 1 to about 10 amino acids consisting of amino acids with inert side chains. Suitable oligopeptides include polyglycine, polyserine, polyproline, polyalanine and oligopeptides consisting of alanyl and/or serinyl and/or prolinyl and/or glycyl amino acid residues. m in structural formula II is an integer from 0 to about 20.

[0172] The peptides, polypeptides and proteins in a multivalent protein can be connected to each other by covalent bonds, linker groups, spacers, cleavage groups or a combination thereof. The linking groups can be the same or different.

[0173] A polypeptide spacer shown in structural formula (II) is a peptide having from about 5 to about 40 amino acid residues. The spacers in a polypeptide multivalent ligand are independently chosen, and may be the same or different. The spacers should allow for flexibility of movement in space for the flanking peptides polypeptides and proteins P, and are therefore typically rich in small amino acids, for example, glycine, serine, proline or alanine. Preferably, peptide spacers contain at least 60%, more preferably at least 80% glycine or alanine. In addition, peptide spacers generally have little or no biological and antigenic activity. Preferred spacers are (Gly-Pro-Gly-Gly)_(x) (SEQ ID NO:81) and (Gly₄-Ser)_(y), wherein x is an integer from about 3 to about 9 and y is an integer from about 1 to about 8. Specific examples of suitable spacers include (Gly₄-Ser)₃ (SEQ ID NO:82). Spacers can also include from one to about four amino acids that create a signal for proteolytic cleavage.

[0174] In another embodiment of the present invention, a TAG sequence is linked to a gene of interest. The TAG sequence serves three purposes: 1) it allows free rotation of the peptide or protein to be isolated so there is no interference from the native protein or signal sequence, i.e. vitellogenin, 2) it provides a “purification handle” to isolate the protein using affinity purification, and 3) it includes a cleavage site to remove the desired protein from the signal and purification sequences. Accordingly, as used herein, a TAG sequence includes a spacer sequence, a purification handle and a cleavage site. The spacer sequences in the TAG proteins contain one or more repeats shown in SEQ ID NO:85. A preferred spacer sequence comprises the sequence provided in SEQ ID NO:86. One example of a purification handle is the gp41 hairpin loop from HIV I. Exemplary gp41 polynucleotide and polypeptide sequences are provided in SEQ ID NO:87 and SEQ ID NO:88, respectively. However, it should be understood that any antigenic region, or otherwise associative regions such as avidin/biotin, may be used as a purification handle, including any antigenic region of gp41. Preferred purification handles are those that elicit highly specific antibodies. Additionally, the cleavage site can be any protein cleavage site known to one of ordinary skill in the art and includes an enterokinase cleavage site comprising the Asp Asp Asp Asp Lys sequence (SEQ ID NO:89) and a furin cleavage site. In one embodiment of the present invention, the TAG sequence comprises a polynucleotide sequence of SEQ ID NO:90.

[0175] Methods of Administering Polynucleotide Cassettes

[0176] In addition to the polynucleotide cassettes described above, the present invention also includes methods of administering the polynucleotide cassettes to an animal, methods of producing a transgenic animal wherein a gene of interest is incorporated into the germline of the animal and methods of producing a transgenic animal wherein a gene of interest is incorporated into cells other than the germline cells of the animal. The polynucleotide cassettes may reside in any vector or delivery solution when administered or may be naked DNA. In one embodiment, a transposon-based vector containing the polynucleotide cassette between two insertion sequences recognized by a transposase is administered to an animal. The polynucleotide cassettes of the present invention may be administered to an animal via any method known to those of skill in the art, including, but not limited to, intraembryonic, intratesticular, intraoviduct, intraovarian, into the duct system of the mammary gland, intraperitoneal, intraarterial, intravenous, topical, oral, nasal, and pronuclear injection methods of administration, or any combination thereof. The polynucleotide cassettes may also be administered within the lumen of an organ, into an organ, into a body cavity, into the cerebrospinal fluid, through the urinary system, through the genitourinary system, through the reproductive system, or through any route to reach the desired cells.

[0177] The polynucleotide cassettes may be delivered through the vascular system to be distributed to the cells supplied by that vessel. For example, the compositions may be placed in the artery supplying the ovary or supplying the fallopian tube to transfect cells in those tissues. In this manner, follicles could be transfected to create a germline transgenic animal. Alternatively, supplying the compositions through the artery leading to the oviduct would preferably transfect the tubular gland and epithelial cells. Such transfected cells could manufacture a desired protein or peptide for deposition in the egg white. Administration of the compositions through the portal vein would target uptake and transformation of hepatic cells. Administration through the urethra and into the bladder would target the transitional epithelium of the bladder. Administration through the vagina and cervix would target the lining of the uterus and the epithelial cells of the fallopian tube. Administration through the internal mammary artery or through the duct system of the mammary gland would transfect secretory cells of the lactating mammary gland to perform a desired function, such as to synthesize and secrete a desired protein or peptide into the milk.

[0178] The polynucleotide cassettes may be administered in a single administration, multiple administrations, continuously, or intermittently. The polynucleotide cassettes may be administered by injection, via a catheter, an osmotic mini-pump or any other method. In some embodiments, a polynucleotide cassette is administered to an animal in multiple administrations, each administration containing the polynucleotide cassette and a different transfecting reagent.

[0179] In a preferred embodiment, the animal is an egg-laying animal, and more preferably, an avian. In one embodiment, between approximately 1 and 150 μg, 1 and 100 μg, 1 and 50 μg, preferably between 1 and 20 μg, and more preferably between 5 and 10 μg of a transposon-based vector containing the polynucleotide cassette is administered to the oviduct of a bird. In a chicken, it is preferred that between approximately 1 and 100 μg, or 5 and 50 μg are administered. In a quail, it is preferred that between approximately S and 10 μg are administered. Optimal ranges depending upon the type of bird and the bird's stage of sexual maturity. Intraoviduct administration of the transposon-based vectors of the present invention result in a PCR positive signal in the oviduct tissue, whereas intravascular administration results in a PCR positive signal in the liver. In other embodiments, the polynucleotide cassettes is administered to an artery that supplies the oviduct or the liver. These methods of administration may also be combined with any methods for facilitating transfection, including without limitation, electroporation, gene guns, injection of naked DNA, and use of dimethyl sulfoxide (DMSO).

[0180] The transposon-based vectors may be administered to the animal at any point during the lifetime of the animal, however, it is preferable that the vectors are administered prior to the animal reaching sexual maturity. The transposon-based vectors are preferably administered to a chicken oviduct between approximately 14 and 16 weeks of age and to a quail oviduct between approximately 5 and 10 weeks of age, more preferably 5 and 8 weeks of age, and most preferably between 5 and 6 weeks of age, when standard poultry rearing practices are used. The vectors may be administered at earlier ages when exogenous hormones are used to induce early sexual maturation in the bird. In some embodiments, the transposon-based vector is administered to an animal's oviduct following an increase in proliferation of the oviduct epithelial cells and/or the tubular gland cells. Such an increase in proliferation normally follows an influx of reproductive hormones in the area of the oviduct. When the animal is an avian, the transposon-based vector is administered to the avian's oviduct following an increase in proliferation of the oviduct epithelial cells and before the avian begins to produce egg white constituents.

[0181] The present invention also includes a method of intraembryonic administration of a transposon-based vector containing a polynucleotide cassette to an avian embryo comprising the following steps: 1) incubating an egg on its side at room temperature for two hours to allow the embryo contained therein to move to top dead center (TDC); 2) drilling a hole through the shell without penetrating the underlying shell membrane; 3) injecting the embryo with the transposon-based vector in solution; 4) sealing the hole in the egg; and 5) placing the egg in an incubator for hatching. Administration of the transposon-based vector can occur anytime between immediately after egg lay (when the embryo is at Stage X) and hatching. Preferably, the transposon-based vector is administered between 1 and 7 days after egg lay, more preferably between 1 and 2 days after egg lay. The transposon-based vectors may be introduced into the embryo in amounts ranging from about 5.0 μg to 10 μg, preferably 1.0 μg to 100 μg. Additionally, the transposon-based vector solution volume may be between approximately 1 μl to 75 μl in quail and between approximately 1 μl to 500 μl in chicken.

[0182] The present invention also includes a method of intratesticular administration of a transposon-based vector containing a polynucleotide cassette including injecting a bird with a composition comprising the transposon-based vector, an appropriate carrier and an appropriate transfection reagent. In one embodiment, the bird is injected before sexual maturity, preferably between approximately 4-14 weeks, more preferably between approximately 6-14 weeks and most preferably between 8-12 weeks old. In another embodiment, a mature bird is injected with a transposon-based vector an appropriate carrier and an appropriate transfection reagent. The mature bird may be any type of bird, but in one example the mature bird is a quail.

[0183] A bird is preferably injected prior to the development of the blood-testis barrier, which thereby facilitates entry of the transposon-based vector into the seminiferous tubules and transfection of the spermatogonia or other germline cells. At and between the ages of 4, 6, 8, 10, 12, and 14 weeks, it is believed that the testes of chickens are likely to be most receptive to transfection. In this age range, the blood/testis barrier has not yet formed, and there is a relatively high number of spermatogonia relative to the numbers of other cell types, e.g., spermatids, etc. See J. Kumaran et al., 1949. Poultry Sci., 29:511-520. See also E. Oakberg, 1956. Am. J. Anatomy, 99:507-515; and P. Kluin et al., 1984. Anat. Embryol., 169:73-78.

[0184] The transposon-based vectors may be introduced into a testis in an amount ranging from about 0.1 μg to 10 μg, preferably 1 μg to 10 μg, more preferably 3 μg to 10 μg. In a quail, about 5 μg is a preferred amount. In a chicken, about 5 μg to 10 μg per testis is preferred. These amounts of vector DNA may be injected in one dose or multiple doses and at one site or multiple sites in the testis. In a preferred embodiment, the vector DNA is administered at multiple sites in a single testis, both testes being injected in this manner. In one embodiment, injection is spread over three injection sites: one at each end of the testis, and one in the middle. Additionally, the transposon-based vector solution volume may be between approximately 1 μl to 75 μl in quail and between approximately 1 μl to 500 μl in chicken. In a preferred embodiment, the transposon-based vector solution volume may be between approximately 20 μl to 60 μl in quail and between approximately 50 μl to 250 μl in chicken. Both the amount of vector DNA and the total volume injected into each testis may be determined based upon the age and size of the bird.

[0185] According to the present invention, the polynucleotide cassette is administered in conjunction with an acceptable carrier and/or transfection reagent. Acceptable carriers include, but are not limited to, water, saline, Hanks Balanced Salt Solution (HBSS), Tris-EDTA (TE) and lyotropic liquid crystals. Transfection reagents commonly known to one of ordinary skill in the art that may be employed include, but are not limited to, the following: cationic lipid transfection reagents, cationic lipid mixtures, polyamine reagents, liposomes and combinations thereof; SUPERFECT®, Cytofectene, BioPORTER®, GenePORTER®, NeuroPORTER®, and perfectin from Gene Therapy Systems; lipofectamine, cellfectin, DMRIE-C oligofectamine, and PLUS reagent from InVitrogen; Xtreme gene, fugene, DOSPER and DOTAP from Roche; Lipotaxi and Genejammer from Strategene; and Escort from SIGMA. In one embodiment, the transfecfion reagent is SUPERFECT®. The ratio of DNA to transfection reagent may vary based upon the method of administration. In one embodiment, a transposon-based vector containing a polynucleotide cassette is administered intratesticularly and the ratio of DNA to transfection reagent can be from 1:1.5 to 1:15, preferably 1:2 to 1:10, all expressed as wt/vol. Transfection may also be accomplished using other means known to one of ordinary skill in the art, including without limitation electroporation, gene guns, injection of naked DNA, and use of dimethyl sulfoxide (DMSO).

[0186] Depending upon the cell or tissue type targeted for transfection, the form of the transposon-based vector may be important. Plasmids harvested from bacteria are generally closed circular supercoiled molecules, and this is the preferred state of a vector for gene delivery because of the ease of preparation. In some instances, transposase expression and insertion may be more efficient in a relaxed, closed circular configuration or in a linear configuration. In still other instances, a purified transposase protein may be co-injected with a transposon-based vector containing the gene of interest for more immediate insertion. This could be accomplished by using a transfection reagent complexed with both the purified transposase protein and the transposon-based vector.

[0187] Testing for and Breeding Animals Carrying the Transgene

[0188] Following administration of a polynucleotide cassette to an animal, DNA is extracted from the animal to confirm integration of the genes of interest. Advantages provided by the present invention include the high rates of integration, or incorporation, and transcription of the gene of interest when administered to a bird via an intraoviduct or intraovary route (including intraarterial administrations to arteries leading to the oviduct or ovary) and contained within a transposon-based vector.

[0189] Actual frequencies of integration can be estimated both by comparative strength of the PCR signal, and by histological evaluation of the tissues by quantitative PCR. Another method for estimating the rate of transgene insertion is the so-called primed in situ hybridization technique (PRINS). This method determines not only which cells carry a transgene of interest, but also into which chromosome the gene has inserted, and even what portion of the chromosome. Briefly, labeled primers are annealed to chromosome spreads (affixed to glass slides) through one round of PCR, and the slides are then developed through normal in situ hybridization procedures. This technique combines the best features of in situ PCR and fluorescence in situ hybridization (FISH) to provide distinct chromosome location and copy number of the gene in question. The 28s rRNA gene will be used as a positive control for spermatogonia to confirm that the technique is functioning properly. Using different fluorescent labels for the transgene and the 28s gene causes cells containing a transgene to fluoresce with two different colored tags.

[0190] Breeding experiments may also be conducted to determine if germline transmission of the transgene has occurred. In a general bird breeding experiment performed according to the present invention, each male bird is exposed to 2-3 different adult female birds for 3-4 days each. This procedure is continued with different females for a total period of 6-12 weeks. Eggs are collected daily for up to 14 days after the last exposure to the transgenic male, and each egg is incubated in a standard incubator. The resulting embryos are examined for transgene presence at day 3 or 4 using PCR.

[0191] Any male producing a transgenic embryo is bred to additional females. Eggs from these females are incubated, hatched, and the chicks tested for the exogenous DNA. Any embryos that die are necropsied and examined directly for the transgene or protein encoded by the transgene, either by fluorescence or PCR. The offspring that hatch and are found to be positive for the exogenous DNA are raised to maturity. These birds are bred to produce further generations of transgenic birds, to verify efficiency of the transgenic procedure and the stable incorporation of the transgene into the germ line. The resulting embryos are examined for transgene presence at day 3 or 4 using PCR.

[0192] It is to be understood that the above procedure can be modified to suit animals other than birds and that selective breeding techniques may be performed to amplify gene copy numbers and protein output.

[0193] Production of Desired Multimeric Proteins in Egg White

[0194] In one embodiment, a transposon-based vector containing a polynucleotide cassette of the present invention may be administered to a bird for production of desired proteins or peptides in the egg white. These trasnposon-based vectors preferably contain one or more of an ovalbumin promoter, an ovomucoid promoter, an ovalbumin signal sequence and an ovomucoid signal sequence. Oviduct-specific ovalbumin promoters are described in B. O'Malley et al., 1987. EMBO J., vol. 6, pp. 2305-12; A. Qiu et al., 1994. Proc. Nat. Acad. Sci. (USA), vol. 91, pp. 4451-4455; D. Monroe et al., 2000. Biochim. Biophys. Acta, 1517 (1):27-32; H. Park et al., 2000. Biochem., 39:8537-8545; and T. Muramatsu et al., 1996. Poult. Avian Biol. Rev., 6:107-123.

[0195] Production of Desired Multimeric Proteins in Egg Yolk

[0196] The present invention is particularly advantageous for production of recombinant peptides and proteins of low solubility in the egg yolk. Such proteins include, but are not limited to, membrane-associated or membrane-bound proteins, lipophilic compounds; attachment factors, receptors, and components of second messenger transduction machinery. Low solubility peptides and proteins are particularly challenging to produce using conventional recombinant protein production techniques (cell and tissue cultures) because they aggregate in water-based, hydrophilic environments. Such aggregation necessitates denaturation and re-folding of the recombinantly-produced proteins, which may deleteriously affect their structure and function. Moreover, even highly soluble recombinant peptides and proteins may precipitate and require denaturation and renaturation when produced in sufficiently high amounts in recombinant protein production systems. The present invention provides an advantageous resolution of the problem of protein and peptide solubility during production of large amounts of recombinant proteins.

[0197] In one embodiment of the present invention, deposition of a desired protein into the egg yolk is accomplished by attaching a sequence encoding a protein capable of binding to the yolk vitellogenin receptor to a gene of interest that encodes a desired protein. This polynucleotide cassette can be used for the receptor-mediated uptake of the desired protein by the oocytes. In a preferred embodiment, the sequence ensuring the binding to the vitellogenin receptor is a targeting sequence of a vitellogenin protein. The invention encompasses various vitellogenin proteins and their targeting sequences. In a preferred embodiment, a chicken vitellogenin protein targeting sequence is used, however, due to the high degree of conservation among vitellogenin protein sequences and known cross-species reactivity of vitellogenin targeting sequences with their egg-yolk receptors, other vitellogenin targeting sequences can be substituted. One example of a construct for use in the transposon-based vectors of the present invention and for deposition of an insulin protein in an egg yolk is a transposon-based vector containing a vitellogenin promoter, a vitellogenin targeting sequence, a TAG sequence, a pro-insulin sequence and a synthetic polyA sequence. The present invention includes, but is not limited to, vitellogenin targeting sequences residing in the N-terminal domain of vitellogenin, particularly in lipovitellin I. In one embodiment, the vitellogenin targeting sequence contains the polynucleotide sequence of SEQ ID NO:77.

[0198] In a preferred embodiment, the transposon-based vector contains a transposase gene operably-linked to a constitutive promoter and a gene of interest operably-linked to a liver-specific promoter and a vitellogenin targeting sequence.

[0199] Isolation and Purification of Desired Multimeric Proteins

[0200] For large-scale production of protein, an animal breeding stock that is homozygous for the transgene is preferred. Such homozygous individuals are obtained and identified through, for example, standard animal breeding procedures or PCR protocols.

[0201] Once expressed, peptides, polypeptides and proteins can be purified according to standard procedures known to one of ordinary skill in the art, including ammonium sulfate precipitation, affinity columns, column chromatography, gel electrophoresis, high performance liquid chromatography, immunoprecipitation and the like. Substantially pure compositions of about 50 to 99% homogeneity are preferred, and 80 to 95% or greater homogeneity are most preferred for use as therapeutic agents.

[0202] In one embodiment of the present invention, the animal in which the desired protein is produced is an egg-laying animal. In a preferred embodiment of the present invention, the animal is an avian and a desired peptide, polypeptide or protein is isolated from an egg white. Egg white containing the exogenous protein or peptide is separated from the yolk and other egg constituents on an industrial scale by any of a variety of methods known in the egg industry. See, e.g., W. Stadelman et al. (Eds.), Egg Science & Technology, Haworth Press, Binghamton, N.Y. (1995). Isolation of the exogenous peptide or protein from the other egg white constituents is accomplished by any of a number of polypeptide isolation and purification methods well known to one of ordinary skill in the art. These techniques include, for example, chromatographic methods such as gel permeation, ion exchange, affinity separation, metal chelation, HPLC, and the like, either alone or in combination. Another means that may be used for isolation or purification, either in lieu of or in addition to chromatographic separation methods, includes electrophoresis. Successful isolation and purification is confirmed by standard analytic techniques, including HPLC, mass spectroscopy, and spectrophotometry. These separation methods are often facilitated if the first step in the separation is the removal of the endogenous ovalbumin fraction of egg white, as doing so will reduce the total protein content to be further purified by about 50%.

[0203] To facilitate or enable purification of a desired protein or peptide, the polynucleotide cassettes may include one or more additional epitopes or domains. Such epitopes or domains include DNA sequences encoding enzymatic, chemical or photolabile cleavage sites including, but not limited to, an enterokinase cleavage site; the glutathione binding domain from glutathione S-transferase; polylysine; hexa-histidine or other cationic amino acids, and sites cleaved by cyanogen bromide, hydroxylamine, formic acid, and acetic acid; thioredoxin; hemagglutinin antigen; maltose binding protein; a fragment of gp41 from HIV; and other purification epitopes or domains commonly known to one of skill in the art. Other proteolytic cleavage sites that may be included in the polynucleotide cassettes are cleavage sites recognized by exopeptidases such as carboxypeptidase A, carboxypeptidase B, aminopeptidase I, and dipeptidylaminopeptidase; endopeptidases such as trypsin, V8-protease, enterokinase, factor Xa, collagenase, endoproteinase, subtilisin, and thombin; and proteases such as Protease 3C IgA protease (Igase) Rhinovirus 3C(preScission)protease. Self-splicing cleavage sites such as inteins may also be included in the polynucleotide cassettes of the present invention.

[0204] In one representative embodiment, purification of desired proteins from egg white utilizes the antigenicity of the ovalbumin carrier protein and particular attributes of a TAG linker sequence that spans ovalbumin and the desired protein. The TAG sequence is particularly useful in this process because it contains 1) a highly antigenic epitope, a fragment of gp41 from HIV, allowing for stringent affinity purification, and, 2) a recognition site for the protease enterokinase immediately juxtaposed to the desired protein. In a preferred embodiment, the TAG sequence comprises approximately 50 amino acids. A representative TAG sequence is provided below. Pro Ala Asp Asp Ala Pro Ala Asp (SEQ ID NO: 90) Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Thr Thr Cys Ile Leu Lys Gly Ser Cys Gly Trp Ile Gly Leu Leu Asp Asp Asp Asp Lys

[0205] The underlined sequences were taken from the hairpin loop domain of HIV gp-41 (SEQ ID NO:87). Sequences in italics represent the cleavage site for enterokinase (SEQ ID NO:89). The spacer sequence upstream of the loop domain was made from repeats of (Pro Ala Asp Asp Ala) (SEQ ID NO:85) to provide free rotation and promote surface availability of the hairpin loop from the ovalbumin carrier protein.

[0206] Isolation and purification of a desired protein is performed as follows:

[0207] 1. Enrichment of the egg white protein fraction containing ovalbumin and the transgenic ovalbumin-TAG-desired protein.

[0208] 2. Size exclusion chromatography to isolate only those proteins within a narrow range of molecular weights (a further enrichment of step 1).

[0209] 3. Ovalbumin affinity chromatography. Highly specific antibodies to ovalbumin will eliminate virtually all extraneous egg white proteins except ovalbumin and the transgenic ovalbumin-TAG-desired protein.

[0210] 4. gp41 affinity chromatography using anti-gp41 antibodies. Stringent application of this step will result in virtually pure transgenic ovalbumin-TAG-desired protein.

[0211] 5. Cleavage of the transgene product can be accomplished in at least one of two ways:

[0212] a. The transgenic ovalbumin-TAG-desired protein is left attached to the gp41 affinity resin (beads) from step 4 and the protease enterokinase is added. This liberates the transgene target protein from the gp41 affinity resin while the ovalbumin-TAG sequence is retained. Separation by centrifugation (in a batch process) or flow through (in a column purification), leaves the desired protein together with enterokinase in solution. Enterokinase is recovered and reused.

[0213] b. Alternatively, enterokinase is immobilized on resin (beads) by the addition of poly-lysine moieties to a non-catalytic area of the protease. The transgenic ovalbumin-TAG-desired protein eluted from the affinity column of step 4 is then applied to the protease resin. Protease action cleaves the ovalbumin-TAG sequence from the desired protein and leaves both entities in solution. The immobilized enterokinase resin is recharged and reused.

[0214] c. The choice of these alternatives is made depending upon the size and chemical composition of the transgene target protein.

[0215] 6. A final separation of either of these two (5a or 5b) protein mixtures is made using size exclusion, or enterokinase affinity chromatography. This step allows for desalting, buffer exchange and/or polishing, as needed.

[0216] Cleavage of the transgene product (ovalbumin-TAG-desired protein) by enterokinase, then, results in two products: ovalbumin-TAG and the desired protein. More specific methods for isolation using the TAG label is provided in the Examples. Some desired proteins may require additions or modifications of the above-described approach as known to one of ordinary skill in the art. The method is scaleable from the laboratory bench to pilot and production facility largely because the techniques applied are well documented in each of these settings.

[0217] It is believed that a typical chicken egg produced by a transgenic animal of the present invention will contain at least 0.001 mg, from about 0.001 to 1.0 mg, or from about 0.001 to 100.0 mg of exogenous protein, peptide or polypeptide, in addition to the normal constituents of egg white (or possibly replacing a small fraction of the latter).

[0218] One of skill in the art will recognize that after biological expression or purification, the desired proteins, fragments thereof and peptides may possess a conformation substantially different than the native conformations of the proteins, fragments thereof and peptides. In this case, it is often necessary to denature and reduce protein and then to cause the protein to re-fold into the preferred conformation. Methods of reducing and denaturing proteins and inducing re-folding are well known to those of skill in the art.

[0219] Production of Multimeric Proteins in Milk

[0220] In addition to methods of producing eggs containing transgenic proteins or peptides, the present invention encompasses methods for the production of milk containing transgenic proteins or peptides. These methods include the administration of a transposon-based vector described above to a mammal. In one embodiment, the transposon-based vector contains a transposase operably-linked to a constitutive promoter and a gene of interest operably-linked to mammary specific promoter. Genes of interest can include, but are not limited to antiviral and antibacterial proteins and immunoglobulins.

[0221] The following examples will serve to further illustrate the present invention without, at the same time, however, constituting any limitation thereof. On the contrary, it is to be clearly understood that resort may be had to various embodiments, modifications and equivalents thereof which, after reading the description herein, may suggest themselves to those skilled in the art without departing from the spirit of the invention.

EXAMPLE 1

[0222] Preparation of Transposon-Based Vector pTnMod

[0223] A vector was designed for inserting a desired coding sequence into the genome of eukaryotic cells, given below as SEQ ID NO:57. The vector of SEQ ID NO:57, termed pTnMod, was constructed and its sequence verified.

[0224] This vector employed a cytomegalovirus (CMV) promoter. A modified Kozak sequence (ACCATG) (SEQ ID NO:5) was added to the promoter. The nucleotide in the wobble position in nucleotide triplet codons encoding the first 10 amino acids of transposase was changed to an adenine (A) or thymine (T), which did not alter the amino acid encoded by this codon. Two stop codons were added and a synthetic polyA was used to provide a strong termination sequence. This vector uses a promoter designed to be active soon after entering the cell (without any induction) to increase the likelihood of stable integration. The additional stop codons and synthetic polyA insures proper termination without read through to potential genes downstream.

[0225] The first step in constructing this vector was to modify the transposase to have the desired changes. Modifications to the transposase were accomplished with the primers High Efficiency forward primer (Hef) Altered transposase (ATS)-Hef 5′ ATCTCGAGACCATGTGTGAACTTGATATTTTACATGATTCTCTTTACC 3′ (SEQ ID NO:91) and Altered transposase-High efficiency reverse primer (Her) 5′ GATTGATCATTATCATAATTTCCCCAAAGCGTAACC 3′ (SEQ ID NO:92, a reverse complement primer). In the 5′ forward primer ATS-Hef, the sequence CTCGAG (SEQ ID NO:93) is the recognition site for the restriction enzyme Xho I, which permits directional cloning of the amplified gene. The sequence ACCATG (SEQ ID NO:5) contains the Kozak sequence and start codon for the transposase and the underlined bases represent changes in the wobble position to an A or T of codons for the first 10 amino acids (without changing the amino acid coded by the codon). Primer ATS-Her (SEQ ID NO:92) contains an additional stop codon TAA in addition to native stop codon TGA and adds a Bcl I restriction site, TGATCA (SEQ ID NO:94), to allow directional cloning. These primers were used in a PCR reaction with pTnLac (p defines plasmid, tn defines transposon, and lac defines the beta fragment of the lactose gene, which contains a multiple cloning site) as the template for the transposase and a FailSafe™ PCR System (which includes enzyme, buffers, dNTP's, MgCl₂ and PCR Enhancer; Epicentre Technologies, Madison, Wis.). Amplified PCR product was electrophoresed on a 1% agarose gel, stained with ethidium bromide, and visualized on an ultraviolet transilluminator. A band corresponding to the expected size was excised from the gel and purified from the agarose using a Zymo Clean Gel Recovery Kit (Zymo Research, Orange, Calif.). Purified DNA was digested with restriction enzymes Xho I (5′) and Bcl 1 (3′) (New England Biolabs, Beverly, Mass.) according to the manufacturer's protocol. Digested DNA was purified from restriction enzymes using a Zymo DNA Clean and Concentrator kit (Zymo Research).

[0226] Plasmid gWhiz (Gene Therapy Systems, San Diego, Calif.) was digested with restriction enzymes Sal I and BamH I (New England Biolabs), which are compatible with Xho I and Bcl I, but destroy the restriction sites. Digested gwhiz was separated on an agarose gel, the desired band excised and purified as described above. Cutting the vector in this manner facilitated directional cloning of the modified transposase (mATS) between the CMV promoter and synthetic polyA.

[0227] To insert the mATS between the CMV promoter and synthetic polyA in gwhiz, a Stratagene T4 Ligase Kit (Stratagene, Inc. La Jolla, Calif.) was used and the ligation set up according to the manufacturer's protocol. Ligated product was transformed into E. coli Top 10 competent cells (Invitrogen Life Technologies, Carlsbad, Calif.) using chemical transformation according to Invitrogen's protocol. Transformed bacteria were incubated in 1 ml of SOC (GIBCO BRL, CAT# 15544-042) medium for 1 hour at 37° C. before being spread to LB (Luria-Bertani media (broth or agar)) plates supplemented with 100 μg/ml ampicillin (LB/amp plates). These plates were incubated overnight at 37° C. and resulting colonies picked to LB/amp broth for overnight growth at 37° C. Plasmid DNA was isolated using a modified alkaline lysis protocol (Sambrook et al., 1989), electrophoresed on a 1% agarose gel, and visualized on a U.V. transilluminator after ethidium bromide staining. Colonies producing a plasmid of the expected size (approximately 6.4 kbp) were cultured in at least 250 ml of LB/amp broth and plasmid DNA harvested using a Qiagen Maxi-Prep Kit (column purification) according to the manufacturer's protocol (Qiagen, Inc., Chatsworth, Calif.). Column purified DNA was used as template for sequencing to verify the changes made in the transposase were the desired changes and no further changes or mutations occurred due to PCR amplification. For sequencing, Perkin-Elmer's Big Dye Sequencing Kit was used. All samples were sent to the Gene Probes and Expression Laboratory (LSU School of Veterinary Medicine) for sequencing on a Perkin-Elmer Model 377 Automated Sequencer.

[0228] Once a clone was identified that contained the desired mATS in the correct orientation, primers CMVf-NgoM IV (5′ TTGCCGGCATCAGATTGGCTAT (SEQ ID NO:95); underlined bases denote NgoM IV recognition site) and Syn-polyA-BstE II (5′ AGAGGTCACCGGGTCAATTCTTCAGCACCTGGTA (SEQ ID NO:96); underlined bases denote BstE II recognition site) were used to PCR amplify the entire CMV promoter, mATS, and synthetic polyA for cloning upstream of the transposon in pTnLac. The PCR was conducted with FailSafe™ as described above, purified using the Zymo Clean and Concentrator kit, the ends digested with NgoM IV and BstE II (New England Biolabs), purified with the Zymo kit again and cloned upstream of the transposon in pTnLac as described below.

[0229] Plasmid pTnLac was digested with NgoM IV and BstE II to remove the ptac promoter and transposase and the fragments separated on an agarose gel. The band corresponding to the vector and transposon was excised, purified from the agarose, and dephosphorylated with calf intestinal alkaline phosphatase (New England Biolabs) to prevent self-annealing. The enzyme was removed from the vector using a Zymo DNA Clean and Concentrator-5. The purified vector and CMVp/mATS/polyA were ligated together using a Stratagene T4 Ligase Kit and transformed into E. coli as described above.

[0230] Colonies resulting from this transformation were screened (mini-preps) as describe above and clones that were the correct size were verified by DNA sequence analysis as described above. The vector was given the name pTnMod (SEQ ID NO:57) and includes the following components:

[0231] Base pairs 1-130 are a remainder of F1(−) on from pBluescriptll sk(−) (Stratagene), corresponding to base pairs 1-130 of pBluescriptll sk(−).

[0232] Base pairs 131-132 are a residue from ligation of restriction enzyme sites used in constructing the vector.

[0233] Base pairs 133-1777 are the CMV promoter/enhancer taken from vector pGWiz (Gene Therapy Systems), corresponding to bp 229-1873 of pGWiz. The CMV promoter was modified by the addition of an ACC sequence upstream of ATG.

[0234] Base pairs 1778-1779 are a residue from ligation of restriction enzyme sites used in constructing the vector.

[0235] Base pairs 1780-2987 are the coding sequence for the transposase, modified from Tn10 (GenBank accession J01829) by optimizing codons for stability of the transposase mRNA and for the expression of protein. More specifically, in each of the codons for the first ten amino acids of the transposase, G or C was changed to A or T when such a substitution would not alter the amino acid that was encoded.

[0236] Base pairs 2988-2993 are two engineered stop codons.

[0237] Base pair 2994 is a residue from ligation of restriction enzyme sites used in constructing the vector.

[0238] Base pairs 2995-3410 are a synthetic polyA sequence taken from the pGWiz vector (Gene Therapy Systems), corresponding to bp 1922-2337 of 10 pGWiz.

[0239] Base pairs 3415-3718 are non-coding DNA that is residual from vector pNK2859.

[0240] Base pairs 3719-3761 are non-coding λ DNA that is residual from pNK2859.

[0241] Base pairs 3762-3831 are the 70 bp of the left insertion sequence recognized by the transposon Tn10.

[0242] Base pairs 3832-3837 are a residue from ligation of restriction enzyme sites used in constructing the vector.

[0243] Base pairs 3838-4527 are the multiple cloning site from pBluescriptll sk(20), corresponding to bp 924-235 of pBluescriptll sk(−). This multiple cloning site may be used to insert any coding sequence of interest into the vector.

[0244] Base pairs 4528-4532 are a residue from ligation of restriction enzyme sites used in constructing the vector.

[0245] Base pairs 4533-4602 are the 70 bp of the right insertion sequence recognized by the transposon Tn10.

[0246] Base pairs 4603-4644 are non-coding λ DNA that is residual from pNK2859.

[0247] Base pairs 4645-5488 are non-coding DNA that is residual from pNK2859.

[0248] Base pairs 5489-7689 are from the pBluescriptll sk(−) base vector—(Stratagene, Inc.), corresponding to bp 761-2961 of pBluescriptll sk(−).

[0249] Completing pTnMod is a pBlueScript backbone that contains a colE I origin of replication and an antibiotic resistance marker (ampicillin).

[0250] It should be noted that all non-coding DNA sequences described above can be replaced with any other non-coding DNA sequence(s). Missing nucleotide sequences in the above construct represent restriction site remnants.

[0251] All plasmid DNA was isolated by standard procedures. Briefly, Escherichia coli containing the plasmid was grown in 500 mL aliquots of LB broth (supplemented with an appropriate antibiotic) at 37° C. overnight with shaking. Plasmid DNA was recovered from the bacteria using a Qiagen Maxi-Prep kit (Qiagen, Inc., Chatsworth, Calif.) according to the manufacturer's protocol. Plasmid DNA was resuspended in 500 μL of PCR-grade water and stored at −20° C. until used.

EXAMPLE 2

[0252] Transposon-Based Vector pTnMCS

[0253] Another transposon-based vector was designed for inserting a desired coding sequence into the genome of eukaryotic cells. This vector was termed pTnMCS and its constituents are provided below. The sequence of the pTnMCS vector is provided in SEQ ID NO:56. The pTnMCS vector contains an avian optimized polyA sequence operably-linked to the transposase gene. The avian optimized polyA sequence contains approximately 75 nucleotides that precede the A nucleotide string.

[0254] Bp 1-130 Remainder of F1 (−) ori of pBluescriptll sk(−) (Stratagene) bpl-130

[0255] Bp 133-1777 CMV promoter/enhancer taken from vector pGWIZ (Gene Therapy Systems) bp 229-1873

[0256] Bp 1783-2991 Transposase, from Tn10 (GenBank accession #J01829) bp 108-1316

[0257] Bp 2992-3344 Non coding DNA from vector pNK2859

[0258] Bp 3345-3387 Lambda DNA from pNK2859

[0259] Bp 3388-3457 70 bp of IS10 left from Tn10

[0260] Bp 3464-3670 Multiple cloning site from pBluescriptII sk(−), thru the XmaI site bp 924-718

[0261] Bp 3671-3715 Multiple cloning site from pBluescriptll sk(−), from the XmaI site thru the XhoI site. These base pairs are usually lost when cloning into pTnMCS bp 717-673

[0262] Bp 3716-4153 Multiple cloning site from pbluescriptII sk(−), from the XhoI site bp 672-235

[0263] Bp 4159-4228 70 bp of IS10 right from Tn10

[0264] Bp 4229-4270 Lambda DNA from pNK2859

[0265] Bp 4271-5114 Non-coding DNA from pNK2859

[0266] Bp 5115-7315 pbluescript sk (−) base vector (Stratagene, Inc.) bp 761-2961.

EXAMPLE 3

[0267] Production of Antibody in Egg White

[0268] A transposon-based vector containing a CMV promoter/cecropin prepro/antibody heavy chain/cecropin pro/Antibody light chain/conalbumin poly A (SEQ ID NO:97) was injected into the oviduct of quail and chickens. A total of 20 birds were injected (10 chickens and 10 quail) and eggs were harvested from the birds once the eggs were laid. Partially purified egg white protein (EW) was then run on a gel under both reducing and non-reducing conditions. FIG. 5 is a picture of the gel. Lanes 1 & 18: molecular weight markers, Lanes 2 and 3: EW #1, non-reduced, reduced, respectively; Lanes 4 and 5: EW #2, non-reduced, reduced, respectively, Lanes 6 and 7: EW #3, non-reduced, reduced, respectively, Lanes 8 and 9: EW #4, non-reduced, reduced, respectively; Lanes 10 and 11: EW #5, non-reduced, reduced, respectively; Lanes 12 and 13: EW #6, non-reduced, reduced, respectively; Lanes 14 and 15: EW #7, non-reduced, reduced, respectively; and Lanes 16 and 17: EW #8 Control, non-reduced, reduced, respectively. Based upon the gel results, the possibility that the egg white in the treated chicken and quail contains antibody produced by the above-mentioned transposon-based vector cannot be excluded.

EXAMPLE 4

[0269] Additional Transpson-Based Vectors for Administration to an Animal

[0270] The following example provides a description of various transposon-based vectors of the present invention and several constructs for insertion into the transposon-based vectors of the present invention. These examples are not meant to be limiting in any way. The constructs for insertion into a transposon-based vector are provided in a cloning vector pTnMCS or pTnMod, both described above.

[0271] pTnMOD (CMV-prepro-HCPro-Lys-CPA) (SEQ ID NO:97)

[0272] Bp 1-4090 from vector pTnMod, bp 1-4090

[0273] Bp 4096-5739 CMV promoter/enhancer taken from vector pGWIZ (Gene therapy systems), bp 230-1864

[0274] Bp 5746-5916 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0275] Bp 5923-7287 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0276] Bp 7288-7302 Pro taken from GenBank accession # X07404, bp 719-733 (includes Lysine)

[0277] Bp 7309-7953 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0278] Bp 7960-8372 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0279] Bp 8374-11973 from cloning vector pTnMod, bp 4091-7690

[0280] pTnMCS(CHOVep-prepro-HCPro-CPA) (SEQ ID NO:98)

[0281] Bp 1-3715 from vectorpTnMCS, bp 1-3715

[0282] Bp 3721-4395 Chicken Ovalbumin enhancer taken from GenBank accession # S82527.1, bp 1-675

[0283] Bp 4402-5738 Chicken Ovalbumin promoter taken from GenBank accession # J00899-M24999, bp 1-1336

[0284] Bp 5745-5915 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0285] Bp 5922-7286 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0286] Bp 7287-7298 Pro taken from GenBank accession # X07404, bp 719-730 (does not include Lysine)

[0287] Bp 7305-7949 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0288] Bp 7956-8363 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0289] Bp 8365-11964 from cloning vector pTnMCS, bp 3716-7315

[0290] pTnMCS(CHOvep-prepro-HCPro-Lys-CPA) (SEQ ID NO:99)

[0291] Bp 1-3715 from vector pTnMCS, bp 1-3715

[0292] Bp 3721-4395 Chicken Ovalbumin enhancer taken from GenBank accession # S82527.1, bp 1-675

[0293] Bp 4402-5738 Chicken Ovalbumin promoter taken from GenBank accession # J00899-M24999, bp 1-1336

[0294] Bp 5745-5915 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0295] Bp 5922-7286 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0296] Bp 7287-7301 Pro taken from GenBank accession # X07404, bp 719-733 (includes Lysine)

[0297] Bp 7308-7952 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0298] Bp 7959-8366 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0299] Bp 8368-11967 from cloning vector pTnMCS, bp 3716-7315

[0300] pTnMCS (CMV-prepro-HCPro-CPA) (SEQ ID NO:100)

[0301] Bp 1-3715 from vector pTnMCS, bp 1-3715

[0302] Bp 3721-5364 CMV promoter/enhancer taken from vector pGWIZ (Gene therapy systems), bp 230-1864

[0303] Bp 5371-5541 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0304] Bp 5548-6912 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0305] Bp 6913-6924 Pro taken from GenBank accession # X07404, bp 719-730 (does not Lysine)

[0306] Bp 6931-7575 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0307] Bp 7582-7989 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0308] Bp 7991-11590 from cloning vector pTnMCS, bp 3716-7315

[0309] pTnMCS (CMV-prepro-HCPro-Lys-CPA) (SEQ ID NO:101)

[0310] Bp 1-3715 from vector pTnMCS, bp 1-3715

[0311] Bp 3721-5364 CMV promoter/enhancer taken from vector pGWIZ (Gene therapy systems), bp 230-1864

[0312] Bp 5371-5541 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0313] Bp 5548-6912 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0314] Bp 6913-6927 Pro taken from GenBank accession # X07404, bp 719-733 (includes Lysine)

[0315] Bp 6934-7578 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0316] Bp 7585-7992 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0317] Bp 7994-11593 from cloning vector pTnMCS, bp 3716-7315

[0318] pTnMod (CHOvep-prepro-HCPro-CPA) (SEQ ID NO:102)

[0319] Bp 1-4090 from vector pTnMod, bp 1-4090

[0320] Bp 4096-4770 Chicken Ovalbumin enhancer taken from GenBank accession # S82527.1, bp 1-675

[0321] Bp 4777-6113 Chicken Ovalbumin promoter taken from GenBank accession # J00899-M24999, bp 1-1336

[0322] Bp 6120-6290 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0323] Bp 6297-7661 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0324] Bp 7662-7673 Pro taken from GenBank accession # X07404, bp 719-730 (does not include Lysine)

[0325] Bp 7680-8324 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0326] Bp 8331-8738 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0327] Bp 8740-12339 from cloning vector pTnMod, bp 3716-7315

[0328] pTnMod (CHOvep-prepro-HCPro-LYS-CPA) (SEQ ID NO:103)

[0329] Bp 1-4090 from vector pTnMod, bp 14090

[0330] Bp 4096-4770 Chicken Ovalbumin enhancer taken from GenBank accession # S82527.1, bp 1-675

[0331] Bp 4777-6113 Chicken Ovalbumin promoter taken from GenBank accession # J00899-M24999, bp 1-1336

[0332] Bp 6120-6290 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0333] Bp 6297-7661 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0334] Bp 7662-7676 Pro taken from GenBank accession # X07404, bp 719-733 (includes Lysine)

[0335] Bp 7683-8327 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0336] Bp 8334-8741 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0337] Bp 8743-12342 from cloning vector pTnMod, bp 3716-7315

[0338] pTnMod (CMV-prepro-HCPro-CPA) (SEQ ID NO:104)

[0339] Bp 1-4090 from vector pTnMod, bp 1-4090

[0340] Bp 4096-5739 CMV promoter/enhancer taken from vector pGWIZ (Gene therapy systems), bp 230-1864

[0341] Bp 5746-5916 Capsite/Prepro taken from GenBank accession # X07404, bp 563-733

[0342] Bp 5923-7287 Heavy Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0343] Bp 7288-7299 Pro taken from GenBank accession # X07404, bp 719-730 (does not include Lysine)

[0344] Bp 7306-7950 Light Chain gene construct taken from antibody RM2 provided by Mark Glassy (Shantha West, Inc)

[0345] Bp 7557-7969 Conalbumin polyA taken from GenBank accession # Y00407, bp 10651-11058

[0346] Bp 7971-11970 from cloning vector pTnMod, bp 3716-7315

[0347] All patents, publications and abstracts cited above are incorporated herein by reference in their entirety. It should be understood that the foregoing relates only to preferred embodiments of the present invention and that numerous modifications or alterations may be made therein without departing from the spirit and the scope of the present invention as defined in the following claims.

1 104 1 15 DNA ARTIFICIAL SEQUENCE Synthetic 1 gcgccagagc cgaaa 15 2 30 DNA ARTIFICIAL SEQUENCE Synthetic 2 gcgccagagc cgaaatggaa agtcttcaag 30 3 78 DNA ARTIFICIAL SEQUENCE Synthetic 3 aatttctcaa ggatattttt cttcgtgttc gctttggttc tggctttgtc aacagtttcg 60 gctgcgccag agccgaaa 78 4 93 DNA ARTIFICIAL SEQUENCE Synthetic 4 aatttctcaa ggatattttt cttcgtgttc gctttggttc tggctttgtc aacagtttcg 60 gctgcgccag agccgaaatg gaaagtcttc aag 93 5 6 DNA ARTIFICIAL SEQUENCE Synthetic 5 accatg 6 6 54 DNA ARTIFICIAL SEQUENCE Synthetic 6 atgctgggca tctggaccct cctacctctg gttcttacgt ctgttgctag atta 54 7 66 DNA ARTIFICIAL SEQUENCE Synthetic 7 atgattcctg ccagatttgc cggggtgctg cttgctctgg ccctcatttt gccagggacc 60 ctttgt 66 8 78 DNA ARTIFICIAL SEQUENCE Synthetic 8 atgggcagag caatggtggc caggctgggg ctggggctgc tgctgctggc actgctccta 60 cccacgcaga tttattcc 78 9 63 DNA ARTIFICIAL SEQUENCE Synthetic 9 atgaatctat cgaacatttc tgcggtaaaa gtattaacac tggtggttag cgctgccatc 60 gct 63 10 390 DNA ARTIFICIAL SEQUENCE Synthetic 10 atgaccatcc ttttccttac tatggttatc tcatacttca gttgcatgaa agctgccccg 60 atgaaagaag ctagtgtaag aggacatggc agcttggctt acccaggtct tcggacccac 120 gggactcttg aaagcctaac tgggcccaat gctggttcaa gaggactgac atcactggcg 180 gacacttttg aacacgtgat agaggagctt ctagatgaag atcaggacat ccagcccagt 240 gaggaaaaca aggatgcgga cttgtacaca tcccgagtca tgctgagcag tcaagtgcct 300 ttggaacccc cactgctctt tctgctcgag gagtacaaaa actacctgga tgctgcaaac 360 atgtccatga gagtccggcg tcactctgac 390 11 144 DNA ARTIFICIAL SEQUENCE Synthetic 11 cgtctttttc tcttatcttt tctcgctttc gctcttttct cgtcggcgat tgctttctcc 60 gacgacgatc cgttgatccg acaagttgta tcgggaaacg atgacaacca tatgttaaac 120 gccgagcatc acttttcact tttt 144 12 415 DNA ARTIFICIAL SEQUENCE Synthetic 12 atgtccatct tgttttatgt gatatttctt gcatatcttc gtggcattca gtcaactaat 60 atggatcaaa ggagtttgcc agaagattca atgaattctc tcattattaa actcattcgg 120 gcagacatct tgaaaaacaa gctttctaag caggtgatgg atgtcaagga aaactatcaa 180 aacatagtgc agaaagtaga ggaccaccag gagatggatg gagatgaaaa tgtgaaatca 240 gacttccagc cagttatttc aatggataca gacctcctaa ggcagcagag acgctacaac 300 tctcctcgag ttctcctaag tgacaacaca ccactggaac caccaccact gtacctcaca 360 gaggattatg ttggaagttc agtggtatta aacagaacct ctcgaaggaa aaggt 415 13 576 DNA ARTIFICIAL SEQUENCE Synthetic 13 atggtgcatc tgactcctga ggagaagtct gccgttactg ccctgtgggg caaggtgaac 60 gtggatgaag ttggtggtga ggccctgggc aggctgctgg tggtctaccc ttggacccag 120 aggttctttg agtcctttgg ggatctgtcc actcctgatg ctgttatggg caaccctaag 180 gtgaaggctc atggcaagaa agtgctcggt gcctttagtg atggcctggc tcacctggac 240 aacctcaagg gcacctttgc cacactgagt gagctgcact gtgacaagct gcacgtggat 300 cctgagaact tcaggctcct gggcaacgtg ctggtctgtg tgctggccca tcactttggc 360 aaagaattca ccccaccagt gcaggctgcc tatcagaaag tggtggctgg tgtggctaat 420 gccctggccc acaagtatca ctaagctcgc tttcttgctg tccaatttct attaaaggtt 480 cctttgttcc ctaagtccaa ctactaaact gggggatatt atgaagggcc ttgagcatct 540 ggattctgcc taataaaaaa catttatttt cattgc 576 14 92 DNA ARTIFICIAL SEQUENCE Synthetic 14 gcatggggac ggcgcttctc cagcgcgggg gctgctttct cctgtgcctt tcgctgctgc 60 tcctgggctg ctgggcggag ctgggcagcg gg 92 15 75 DNA ARTIFICIAL SEQUENCE Synthetic 15 cgaaacgatt caaaacctct ttactgccgt tatttgctgg atttttattg ctgttttatt 60 tggttctggc aggac 75 16 377 DNA ARTIFICIAL SEQUENCE Synthetic 16 ggagtctggg ggaggcttag tgcagcctgg agagtccctg aaactctcct gtgaatccaa 60 tgaatacgaa ttcccttccc atgacatgtc ttgggtccgc aagactccgg agaagaggct 120 ggagttggtc gcagccatta atagtgatgg tggtagcacc tactatccag acaccatgga 180 gagacgattc atcatctcca gagacaatac caagaagacc ctgtacctgc aaatgagcag 240 tctgaggtct gaggacacag ccttgtatta ctgtgcaaga cacacgatga gcaaaagtta 300 ctgtgagctc aaactaaaac ctcctgcaga gcatccagga ccagcagggg gcgcggagag 360 acacagagtt gtgaaat 377 17 310 DNA ARTIFICIAL SEQUENCE Synthetic 17 acatccattc ttctgtgagt ttcactcgaa gagcagcgtg tcactgcgga caagccagcc 60 agctcaccat ggctggacct cccagggtac cagacctctg ggaactggcc ctgagcctca 120 cttcacggac acaggctgcc cgccaaagtg ggtctcagag caacagtgtg tgcattgctc 180 gtcacatctt cctcttgctt tgcatgactg actacaccca agaagtgtgc ccctgggagg 240 aaagcatatt tggcaaccag atcataataa aatcagaaat gcagcaaacc tttaaaatat 300 ccagacttgg 310 18 31 DNA ARTIFICIAL SEQUENCE Synthetic 18 tggaagcaag agggagtatg ctaacttcat g 31 19 16 DNA ARTIFICIAL SEQUENCE Synthetic 19 atcaattaca agaggg 16 20 69 DNA ARTIFICIAL SEQUENCE Synthetic 20 atgaagttmg catactccct cttgcttcca ttggcaggag tcagtgcttc agtkatcaat 60 tacaagaga 69 21 39 DNA ARTIFICIAL SEQUENCE Synthetic 21 aattcttaat taattattgt ggtgtcacaa taacttttc 39 22 96 DNA ARTIFICIAL SEQUENCE Synthetic 22 ccccccggat ccatggccgc taaattcgtc gtggttctgg ccgcttgcgt cgccctgagc 60 cactcggcta tggtgcgccg caagaagaac ggctac 96 23 60 DNA ARTIFICIAL SEQUENCE Synthetic 23 ccccccggat ccatgaaact cctggtcgtg ttcgccatgt gcgtgcccgc tgccagcgct 60 24 38 DNA ARTIFICIAL SEQUENCE Synthetic 24 cagtgtacgg cggctcgagg cagaagtccg gacgcata 38 25 289 DNA ARTIFICIAL SEQUENCE Synthetic 25 gaattcatta tcagcacgga ccagatttct ggatcaggat agaagtctga cgtttacggt 60 tttcgaagca cagaacgcat tcgttagcgt aagtgtcacc gtcggtaccg caaaccggac 120 ggtattccag agtgcaaccg ttcagttcgt tgtagcattt agcttcacga cccagagagt 180 ccatggatcc cccttccgct gtcttctcag ttccaagcat tgcgattttg ttaagcaacg 240 cactctcgat tcgtagagcc tcgttgcgtt tgtttgcacg aaccatatg 289 26 50 DNA ARTIFICIAL SEQUENCE Synthetic 26 ttcacaggca ggtttttgta gagaggggca tgtcatagtc ctcactgtgg 50 27 309 DNA ARTIFICIAL SEQUENCE Synthetic 27 aagcttctcg tgaaaaccaa cccaattagt tagtattgca ttctgtgtac tatagtttgg 60 aatattaaaa atattttaaa atacctccat tttgcttatc cttttagtga agatgatacc 120 tgcaaaagac atggctaaag ttatgattgt catgttggca atttgttttc ttacaaaatc 180 ggatgggaaa tctgttaagt aagtactgtt ttgccttgga attggatttt taatgttgac 240 tttatcattt cgaagtgggg agctaatggg aagtggccct ctctgtttct cttcttccca 300 ggaagagat 309 28 78 DNA ARTIFICIAL SEQUENCE Synthetic 28 atggctacag gctcccggac gtccctgctc ctggcttttg gcctgctctg cctgccctgg 60 cttcaagagg gcagtgcc 78 29 54 DNA ARTIFICIAL SEQUENCE Synthetic 29 atgaggtctt tgctaatctt ggtgctttgc ttcctgcccc tggctgctct gggg 54 30 96 DNA ARTIFICIAL SEQUENCE Synthetic 30 atgcacctga gaatccacgc gagacggaac cctcctcgcc ggccggcctg gacgcttggg 60 atctggtccc ttttctgggg atgtatcgtc agctct 96 31 150 DNA ARTIFICIAL SEQUENCE Synthetic 31 atggccatta gtggagtccc tgtgctagga tttttcatca tagctgtgct gatgagcgct 60 caggaatcat gggctatcaa agaagaacat gtgatcatcc aggccgagtt ctatctgaat 120 cctgaccaat caggcgagtt tatgtttgac 150 32 79 DNA ARTIFICIAL SEQUENCE Synthetic 32 aggggggatc cccggagacc ttcgggtagc aactgtcacc ttgatgctgg cgatcctgag 60 ctcctcactg gctgagggc 79 33 87 DNA ARTIFICIAL SEQUENCE Synthetic 33 atggtgtgtc tgaggctccc tggaggctcc tgcatggcag ttctgacagt gacactgatg 60 gtgctgagct ccccactggc tttggct 87 34 4045 DNA ARTIFICIAL SEQUENCE Synthetic 34 gaacgattta aggagcgaat actactggta aactaatgga agaaatctgc tgcaccactg 60 gatattggga gtgtgtggca tgcatcctca tcatcaggaa actctaaaaa agaaccgagt 120 ggtgctagcc aaacagctgt tgttgagcga attgttagaa catcttctgg agaaggacat 180 catcaccttg gaaatgaggg agctcatcca ggccaaagtg ggcagtttca gccagaatgt 240 ggaactcctc aacttgctgc ctaagagggg tccccaagct tttgatgcct tctgtgaagc 300 actgagggag accaagcaag gccacctgga ggatatgttg ctcaccaccc tttctgggct 360 tcagcatgta ctcccaccgt tgagctgtga ctacgacttg agtctccctt ttccggtgtg 420 tgagtcctgt cccctttaca agaagctccg cctgtcgaca gatactgtgg aacactccct 480 agacaataaa gatggtcctg tctgccttca ggtgaagcct tgcactcctg aattttatca 540 aacacacttc cagctggcat ataggttgca gtctcggcct cgtggcctag cactggtgtt 600 gagcaatgtg cacttcactg gagagaaaga actggaattt cgctctggag gggatgtgga 660 ccacagtact ctagtcaccc tcttcaagct tttgggctat gacgtccatg ttctatgtga 720 ccagactgca caggaaatgc aagagaaact gcagaatttt gcacagttac ctgcacaccg 780 agtcacggac tcctgcatcg tggcactcct ctcgcatggt gtggagggcg ccatctatgg 840 tgtggatggg aaactgctcc agctccaaga ggtttttcag ctctttgaca acgccaactg 900 cccaagccta cagaacaaac caaaaatgtt cttcatccag gcctgccgtg gaggtgctat 960 tggatccctt gggcacctcc ttctgttcac tgctgccacc gcctctcttg ctctatgaga 1020 ctgatcgtgg ggttgaccaa caagatggaa agaaccacgc aggatcccct gggtgcgagg 1080 agagtgatgc cggtaaagaa aagttgccga agatgagact gcccacgcgc tcagacatga 1140 tatgcggcta tgcctgcctc aaagggactg ccgccatgcg gaacaccaaa cgaggttcct 1200 ggtacatcga ggctcttgct caagtgtttt ctgagcgggc ttgtgatatg cacgtggccg 1260 acatgctggt taaggtgaac gcacttatca aggatcggga aggttatgct cctggcacag 1320 aattccaccg gtgcaaggag atgtctgaat actgcagcac tctgtgccgc cacctctacc 1380 tgttcccagg acaccctccc acatgatgtc acctccccat catccacgcc aagtggaagc 1440 cactggacca caggaggtgt gatagagcct ttgatcttca ggatgcacgg tttctgttct 1500 gccccctcag ggatgtggga atctcccaga cttgtttcct gtgcccatca tctctgcctt 1560 tgagtgtggg actccaggcc agctcctttt ctgtgaagcc ctttgcctgt agagccagcc 1620 ttggttggac ctattgccag gaatgtttca gctgcagttg aagagcctga caagtgaagt 1680 tgtaaacaca gtgtggttat ggggagaggg catataaatt ccccatattt gtgttcagtt 1740 ccagcttttg tagatggcac tttagtgatt gcttttatta cattagttaa gatgtctgag 1800 agaccatctc ctatctttta tttcattcat atcctccgcc ctttttgtcc tagagtgaga 1860 gtttggaagg tgtccaaatt taatgtagac attatctttt ggctctgaag aagcaaacat 1920 gactagagac gcaccttgct gcagtgtcca gaagcggcct gtgcgttccc ttcagtactg 1980 cagcgccacc cagtggaagg acactcttgg ctcgtttggg ctcaaggcac cgcagcctgt 2040 cagccaacat tgccttgcat ttgtacctta ttgatctttg cccatggaag tctcaaagat 2100 ctttcgttgg ttgtttctct gagctttgtt actgaaatga gcctcgtggg gagcatcaga 2160 gaaggccagg aagaatggtg tgtttcccta gactctgtaa ccacctctct gtctttttcc 2220 ttcctgagaa acgtccatct ctctccctta ctattcccac tttcattcaa tcaacctgca 2280 cttcatatct agatttctag aaaagcttcc tagcttatct ccctgcttca tatctctccc 2340 ttctttacct tcatttcatc ctgttggctg ctgccaccaa atctgtctag aatcctgctt 2400 tacaggatca tgtaaatgct caaagatgta atgtagttct ttgttcctgc tttctctttc 2460 agtattaaac tctcctttga tattatgtgg cttttatttc agtgccatac atgttattgt 2520 tttcaaccta gaaaccttta tccctgctta tctgaaactt cccaacttcc ctgttcttta 2580 agactttttt tttttttttt tttttttttg agacagagtc tcgctctgtc gcccaggctg 2640 gagggcagtg gcacgatctc agctcactgc aagctccaac tcccgggttc acgccattct 2700 cctgcctcag ccttccaagt agctgggact acaggtgccc gccaccgtgc ccggctaatt 2760 tttttgtatt tttagtagag acagggtttc accatgttag ccgggatggt cttgatctcc 2820 tgacctcatg atccacccac ctcagcctcc caaagtgttg ggattacagg cgtgagccac 2880 tgcgcccggg caagaccttt ttttaaaaaa aaaaaaaaaa aaacttccat tctttcttcc 2940 tccagtctgt tctcacataa cagagtagtt ttggttttta attttttttg gttgtttgct 3000 gttttttgtt ttttaaggtg agttctcact atgtttctca gactggtctc gaactcctgg 3060 cctcaagcca tcttcccgcc tcagcctctc aaatagctgg gcttacaggc atgagccacc 3120 acacctggcc aggatttggt tgtttaaata taaatctgat cacccccctg cttagaaccc 3180 ttctgctttc tattacccct catttaaaat gtaaactctt caccttggtt tatgagaact 3240 ggttcttgcc ttccccttga acctcattaa atggtgattt cttgctaagc tccagcccga 3300 gtggtctcct ctcagcttct aattttgtgc tctttcctgc ccttttcctg ggccttctca 3360 gctctccacc cccaccactc ttgactcagg tggtgtcctt cttcctcaag tcttgacaat 3420 tcccgggccc ttcagtccct gagcagtcta cttctgtgtc tgtcaccaca tcttgtcttt 3480 tcccctcatt gcatttattg cagtttatat atatgctact tttacttgtt catttctgtc 3540 tcccctacca ggctgtaaat gagggcagaa accttgtttg ttttattcac catcatgtac 3600 caagtgcttg gcacatagtg ggccttcatt aaatgtttgt tgaataaaag agggaagaag 3660 gcaagccaac cttagctaca atcctacctt ttgataaaat gttccttttg acaatataca 3720 cggattatta tttgtacttt gtttttccat gtgttttgct tttatccact ggcattttta 3780 gctccttgaa gacatatcat gtgtgagata acttccttca catctcccat ggtccctagc 3840 aaaatgctag gcctgtagta gtcaaggtgc tcaataaata tttgtttggg tggtttgtga 3900 gccttgctgc caagtcctgc ctttgggtcg acatagtatg gaagtatttg agagagagaa 3960 cctttccact cccactgcca ggattttgta ttgccatcgg gtgccaaata aatgctcata 4020 tttattaaaa aaaaaaaaaa aaaaa 4045 35 501 DNA ARTIFICIAL SEQUENCE Synthetic 35 tccagatcat ctgtcctcac caccaaggcc atggtgtctt cagcgactat ctgcagtttg 60 ctactcctca gcatgctctg gatggacatg gccatggcag gttccagctt cttgagccca 120 gagcaccaga aagcccagca gagaaaggaa tccaagaagc caccagctaa actgcagcca 180 cgagctctgg aaggctggct ccacccagag gacagaggac aagcagaaga ggcagaggag 240 gagctggaaa tcaggttcaa tgctcccttc gatgttggca tcaagctgtc aggagctcag 300 taccagcagc atggccgggc cctgggaaag tttcttcagg atatcctctg ggaagaggtc 360 aaagaggcgc cagctaacaa gtaaccactg acaggactgg tccctgtact ttcctcctaa 420 gcaagaactc acatccagct tctgcctcct ctgcaactcc cagcactctc ctgctgactt 480 acaaataaat gttcaagctg t 501 36 70 DNA ARTIFICIAL SEQUENCE Synthetic 36 atgaagctgc ttgcaatggt tgcactgctg gtcaccatct gtagcctaga aggagctttg 60 gttcggagac 70 37 70 DNA ARTIFICIAL SEQUENCE Synthetic 37 atgaagctgc ttgcaatggt tgcactgctg gtcaccatct gtagcctaga aggagctttg 60 gttcggagac 70 38 99 DNA ARTIFICIAL SEQUENCE Synthetic 38 atggccttgc caacggctcg acccctgttg gggtcctgtg ggacccccgc cctcggcagc 60 ctcctgttcc tgctcttcag cctcggatgg gtgcagccc 99 39 72 DNA ARTIFICIAL SEQUENCE Synthetic 39 atgccgcgcc tgttctccta cctcctaggt gtctggctgc tcctgagcca acttcccaga 60 gaaatcccag gc 72 40 75 DNA ARTIFICIAL SEQUENCE Synthetic 40 atgacagcat cacttgtcgt tttaccatcg ctttggttaa tattaattat ttttactgca 60 ccctatactc actgt 75 41 388 DNA ARTIFICIAL SEQUENCE Synthetic 41 atgaaagtcc tgctttgtga cctgctgctg ctcagtctct tctccagtgt gttcagcagt 60 tgtcagaggg actgtctcac atgccaggag aagctccacc cagccctgga cagcttcgac 120 ctggaggtgt gcatcctcga gtgcgaagag aaggtcttcc ccagccccct ctggactcca 180 tgcaccaagg tcatggccag gagctcttgg cagctcagcc ctgccgcccc agagcatgtg 240 gcggctgctc tctaccagcc gagagcttcg gagatgcagc atctgcggcg aatgccccga 300 gtccggagct tgttccagga gcaggaagag cccgagcctg gcatggagga ggctggtgag 360 atggagcaga agcagctgca gaagagat 388 42 76 DNA ARTIFICIAL SEQUENCE Synthetic 42 aattcatgaa gtgggttact ttcatctctt tgttgttctt gttctcttct gcttactcta 60 gaggtgtttt cagacg 76 43 72 DNA ARTIFICIAL SEQUENCE Synthetic 43 atgaagtggg ttactttcat ctctttgttg ttcttgttct cttctgctta ctctagaggt 60 gttttcagac gc 72 44 1731 DNA ARTIFICIAL SEQUENCE Synthetic 44 gaattctcaa tggcaaaggc aagtgtacat tataaatagc aaaacagctg gcttggacca 60 tgttgccggc cagtcaccca gttgagggat ttgaatgaca tcataaccct caagagggta 120 ttgctagcca gctggtgtta tttagaatac acaaaaatca gagaaagaaa acacactctg 180 gcacacagac tccctctgtc atacacacac acacacacac acacacacac acacacacac 240 agaggtttga gttatatgga aaattcaaac aacaggaaaa ttgtttgccc cccaggtacc 300 cttctcccag agtggtgggg tggggagggg acagtgacag gcagcctagt agaagaataa 360 agaaaaatgt tctatttcag ttgggtttta cagctcggca tagtctttgc ctcatcgcag 420 gagaaaaagt atgagacagt gccctaaagg gaccaatcca atgctgcctg cccctccata 480 cgttctagga aatgagatca cacccctcac ttggcaactg ggacaagggg tcacccgagt 540 gctgtcttcc aatctacttt accccagtca cttcagggtt aaaattgtag agtttgctgg 600 agagggtctt atcgtccttt ctttcttttt ttgttttaaa taatgcattt gctctagaat 660 ctaaaattgc tctcccatcc cccatattcc tttaatactg gtaaggtgta ttagcagacg 720 tttgtgtctt catgcccagc agaaagttaa tcagaaaaca gatccttatt ttctatggca 780 gcataagtat tttaatgtct gcgaaccctg tcagtaacac acattctttt aagggaaaaa 840 aatgcttctg tgctctagtt ttaaaatgca aaggtatgat gttatttgtc accatgccca 900 aaaaagtcct tactcaataa ctttgccaga agagggagag agagagaagg caaatgttcc 960 cccagctgtt tcctgtctac agtgtctgtg ttttgtagat aaatgtgagg attttgtgta 1020 aatccctctt ctgtttgcta aatctcactg tcactgctaa attcagagca gatagagcct 1080 gcgcaatgga ataaagtcct caaaattgaa atgtgacatt gctctcaaca tctcccatct 1140 ctctggattt ctttttgctt cattattcct gctaaccaat tcattttcag actttgtact 1200 tcagaagcaa tgggaaaaat cagcagtctt ccaacccaat tatttaagtg ctgcttttgt 1260 gatttcttga aggtaaatat ttcttactct ttgaagtcat tggggaattc ggatcccact 1320 gtaataatag catctttcat ttccgtagta aacgtttcta gatattttgt ctcaattcat 1380 tgaaatagga acccataaag aaaggggttc agggaggact cctccaaaga tccacagtag 1440 ccaggggaat aaacacaggt tgttggatgc cgagacacgc tccatccaca actccctgct 1500 gggttctcat gtactctatt ggcttctgtg ctgggtagtc ctgattaatg acagtcgtgg 1560 aatcgtggga gtcaatgcac ttctgtccca ccccactccc cttgcaagga tcaaggagga 1620 aacctgaacc tccctctgtt tcttgggcag gtgaagatgc acaccatgtc ctcctcgcat 1680 ctcttctacc tggcgctgtg cctgctcacc ttcaccagct ctgccacggc t 1731 45 122 DNA ARTIFICIAL SEQUENCE Synthetic 45 atgaagccaa ttcaaaaact cctagctggc cttattctac tgacttcgtg cgtggaaggc 60 tgctccagcc agcactggtc ctatggactg cgccctggag gaaagagaga tgccgaaaat 120 tt 122 46 268 DNA ARTIFICIAL SEQUENCE Synthetic 46 atgagatttc cttcaatttt tactgcagtt ttattcgcag catcctccgc attagctgct 60 ccagtcaaca ctacaacaga agatgaaacg gcacaaattc cggctgaagc tgtcatcggt 120 tacttagatt tagaagggga tttcgatgtt gctgttttgc cattttccaa cagcacaaat 180 aacgggttat tgtttataaa tactactatt gccagcattg ctgctaaaga agaaggggta 240 tctttggata aaagagaggc tgaagctt 268 47 74 DNA ARTIFICIAL SEQUENCE Synthetic 47 atgaagtggg taacctttat ttcccttctt tttctcttta gctcggctta ttccaggggt 60 gtgtttcgtc gaga 74 48 366 DNA ARTIFICIAL SEQUENCE Synthetic 48 atgaagatgg tctcctcctc gcgcctccgc tgcctcctcg tgctcctgct gtccctgacc 60 gcctccatca gctgctcctt cgccggacag agagactcca aactccgcct gctgctgcac 120 cggtacccgc tgcagggctc caaacaggac atgactcgct ccgccttggc cgagctgctc 180 ctgtcggacc tcctgcaggg ggagaacgag gctctggagg aggagaactt ccctctggcc 240 gaaggaggac ccgaggacgc ccacgccgac ctagagcggg ccgccagcgg ggggcctctg 300 ctcgcccccc gggagagaaa ggccggctgc aagaacttct tctggaaaac cttcacctcc 360 tgctga 366 49 1428 DNA ARTIFICIAL SEQUENCE Synthetic 49 atggccgggc gagggggcag cgcgctgctg gctctgtgcg gggcactggc tgcctgcggg 60 tggctcctgg gcgccgaagc ccaggagccc ggggcgcccg cggcgggcat gaggcggcgc 120 cggcggctgc agcaagagga cggcatctcc ttcgagtacc accgctaccc cgagctgcgc 180 gaggcgctcg tgtccgtgtg gctgcagtgc accgccatca gcaggattta cacggtgggg 240 cgcagcttcg agggccggga gctcctggtc atcgagctgt ccgacaaccc tggcgtccat 300 gagcctggtg agcctgaatt taaatacatt gggaatatgc atgggaatga ggctgttgga 360 cgagaactgc tcattttctt ggcccagtac ctatgcaacg aataccagaa ggggaacgag 420 acaattgtca acctgatcca cagtacccgc attcacatca tgccttccct gaacccagat 480 ggctttgaga aggcagcgtc tcagcctggt gaactcaagg actggtttgt gggtcgaagc 540 aatgcccagg gaatagatct gaaccggaac tttccagacc tggataggat agtgtacgtg 600 aatgagaaag aaggtggtcc aaataatcat ctgttgaaaa atatgaagaa aattgtggat 660 caaaacacaa agcttgctcc tgagaccaag gctgtcattc attggattat ggatattcct 720 tttgtgcttt ctgccaatct ccatggagga gaccttgtgg ccaattatcc atatgatgag 780 acgcggagtg gtagtgctca cgaatacagc tcctccccag atgacgccat tttccaaagc 840 ttggcccggg catactcttc tttcaacccg gccatgtctg accccaatcg gccaccatgt 900 cgcaagaatg atgatgacag cagctttgta gatggaacca ccaacggtgg tgcttggtac 960 agcgtacctg gagggatgca agacttcaat taccttagca gcaactgttt tgagatcacc 1020 gtggagctta gctgtgagaa gttcccacct gaagagactc tgaagaccta ctgggaggat 1080 aacaaaaact ccctcattag ctaccttgag cagatacacc gaggagttaa aggatttgtc 1140 cgagaccttc aaggtaaccc aattgcgaat gccaccatct ccgtggaagg aatagaccac 1200 gatgttacat ccgcaaagga tggtgattac tggagattgc ttatacctgg aaactataaa 1260 cttacagcct cagctccagg ctatctggca ataacaaaga aagtggcagt tccttacagc 1320 cctgctgctg gggttgattt tgaactggag tcattttctg aaaggaaaga agaggagaag 1380 gaagaattga tggaatggtg gaaaatgatg tcagaaactt taaatttt 1428 50 69 DNA ARTIFICIAL SEQUENCE Synthetic 50 atggctctct cactcttcac tgttggacaa ttaattttct tattttggac actcagaatc 60 actgaagcc 69 51 106 DNA ARTIFICIAL SEQUENCE Synthetic 51 atgaacaaac tagcaattct cgctatcatc gctatggtac ttttcagcgc aaacgccttc 60 agactccaaa gcagattgag atcaaatatg gaagcttctg ccagag 106 52 261 DNA ARTIFICIAL SEQUENCE Synthetic 52 atggtcagtg tgtgcaggct cttgctggtt gctgccttgc tgctgtgttt gcaagcacag 60 ctgtctttct ctcagcactg gtctcatggc tggtaccctg gaggaaagag agaaatcgac 120 tcctacagct caccagagat atctggggag attaaactgt gtgaagcggg agaatgcagc 180 tatctcaggc cactgaggac caacatccta aagagcatcc tgattgacac ccttgcaagg 240 aaattccaaa agaggaaatg a 261 53 304 DNA ARTIFICIAL SEQUENCE Synthetic 53 tgtgttttgt agataaatgt gaggattttc tctaaatccc tcttctgctt gctaaatctc 60 actgtcgctg ctaaattcag agcagataga gcctgcgcaa tcgaaataaa gtcctcaaaa 120 ttgaaatgtg actttgctct aacatctccc atctctctgg atttcttttt gcctcattat 180 tcctgcccac caattcattt ccagactttg tacttcagaa gcgatgggga aaatcagcag 240 tcttccaact caattattta agatctgcct ctgtgacttc ttgaagataa agatacacat 300 catg 304 54 81 DNA ARTIFICIAL SEQUENCE Synthetic 54 atgtcaggcc cgaggacgtg cttctgtcta ccgtcggctc ttgtactagt actgctgagt 60 ctcagcactt cggcactagg g 81 55 474 PRT ARTIFICIAL SEQUENCE Synthetic 55 Met Ser Pro Ala Ala Gln Leu Ala Lys Ala Ala Ala Arg Ser Thr Cys 1 5 10 15 Met Thr Arg Leu Pro Ser Gly Ile Arg Val Ala Thr Ala Pro Ser Asn 20 25 30 Ser His Phe Ala Ala Val Gly Val Tyr Val Asp Ala Gly Pro Ile Tyr 35 40 45 Glu Thr Ser Ile Asp Arg Gly Val Ser His Phe Val Ser Ser Leu Ala 50 55 60 Phe Lys Ser Thr His Gly Ala Thr Glu Ser Gln Val Leu Lys Thr Met 65 70 75 80 Ala Gly Leu Gly Gly Asn Leu Phe Cys Thr Ala Thr Arg Glu Ser Ile 85 90 95 Leu Tyr Gln Gly Ser Val Leu His His Asp Leu Pro Arg Thr Val Gln 100 105 110 Leu Leu Ala Asp Thr Thr Leu Arg Pro Ala Leu Thr Glu Glu Glu Ile 115 120 125 Ala Glu Arg Arg Ala Thr Ile Ala Phe Glu Ala Glu Asp Leu His Ser 130 135 140 Arg Pro Asp Ala Phe Ile Gly Glu Met Met His Ala Val Ala Phe Gly 145 150 155 160 Gly Arg Gly Leu Gly Asn Ser Ile Phe Cys Glu Pro Gln Arg Ala Arg 165 170 175 Asn Met Thr Ser Asp Thr Ile Arg Glu Tyr Phe Ala Thr Tyr Leu His 180 185 190 Pro Ser Arg Met Val Val Ala Gly Thr Gly Val Ala His Ala Glu Leu 195 200 205 Val Asp Leu Val Ser Lys Ala Phe Val Pro Ser Ser Thr Arg Ala Pro 210 215 220 Ser Ser Val Thr His Ser Asp Ile Glu Thr Ala Tyr Val Gly Gly Ser 225 230 235 240 His Gln Leu Val Ile Pro Lys Pro Pro Pro Thr His Pro Asn Tyr Glu 245 250 255 Gln Thr Leu Thr His Val Gln Val Ala Phe Pro Val Pro Pro Phe Thr 260 265 270 His Pro Asp Met Phe Pro Val Ser Thr Leu Gln Val Leu Met Gly Gly 275 280 285 Gly Gly Ala Phe Ser Ala Gly Gly Pro Gly Lys Gly Met Tyr Ser Arg 290 295 300 Leu Tyr Thr Asn Val Leu Asn Arg Tyr Arg Trp Met Glu Ser Cys Ala 305 310 315 320 Ala Phe Gln His Ala Tyr Ser Ser Thr Ser Leu Phe Gly Ile Ser Ala 325 330 335 Ser Cys Val Pro Ser Phe Asn Pro His Leu Cys Asn Val Leu Ala Gly 340 345 350 Glu Phe Val His Met Ala Arg Asn Leu Ser Asp Glu Glu Val Ala Arg 355 360 365 Ala Lys Asn Gln Leu Lys Ser Ser Leu Leu Met Asn Leu Glu Ser Gln 370 375 380 Val Ile Thr Val Glu Asp Ile Gly Arg Gln Val Leu Ala Gln Asn Gln 385 390 395 400 Arg Leu Glu Pro Leu Glu Leu Val Asn Asn Ile Ser Ala Val Thr Arg 405 410 415 Asp Asp Leu Val Arg Val Ala Glu Ala Leu Val Ala Lys Pro Pro Thr 420 425 430 Met Val Ala Val Gly Glu Asp Leu Thr Lys Leu Thr Asp Ile Lys Glu 435 440 445 Thr Leu Ala Ala Phe Asn Ala Ser Gly Glu Ala Leu Gln Pro Val Gly 450 455 460 Ser Ala Gly Ser Phe Gly Arg Val Thr Met 465 470 56 7315 DNA ARTIFICIAL SEQUENCE Synthetic 56 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgcga actcgatatt 1800 ttacacgact ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg aggggatcgc 3000 tctagagcga tccgggatct cgggaaaagc gttggtgacc aaaggtgcct tttatcatca 3060 ctttaaaaat aaaaaacaat tactcagtgc ctgttataag cagcaattaa ttatgattga 3120 tgcctacatc acaacaaaaa ctgatttaac aaatggttgg tctgccttag aaagtatatt 3180 tgaacattat cttgattata ttattgataa taataaaaac cttatcccta tccaagaagt 3240 gatgcctatc attggttgga atgaacttga aaaaaattag ccttgaatac attactggta 3300 aggtaaacgc cattgtcagc aaattgatcc aagagaacca acttaaagct ttcctgacgg 3360 aatgttaatt ctcgttgacc ctgagcactg atgaatcccc taatgatttt ggtaaaaatc 3420 attaagttaa ggtggataca catcttgtca tatgatcccg gtaatgtgag ttagctcact 3480 cattaggcac cccaggcttt acactttatg cttccggctc gtatgttgtg tggaattgtg 3540 agcggataac aatttcacac aggaaacagc tatgaccatg attacgccaa gcgcgcaatt 3600 aaccctcact aaagggaaca aaagctggag ctccaccgcg gtggcggccg ctctagaact 3660 agtggatccc ccgggctgca ggaattcgat atcaagctta tcgataccgc tgacctcgag 3720 ggggggcccg gtacccaatt cgccctatag tgagtcgtat tacgcgcgct cactggccgt 3780 cgttttacaa cgtcgtgact gggaaaaccc tggcgttacc caacttaatc gccttgcagc 3840 acatccccct ttcgccagct ggcgtaatag cgaagaggcc cgcaccgatc gcccttccca 3900 acagttgcgc agcctgaatg gcgaatggaa attgtaagcg ttaatatttt gttaaaattc 3960 gcgttaaatt tttgttaaat cagctcattt tttaaccaat aggccgaaat cggcaaaatc 4020 ccttataaat caaaagaata gaccgagata gggttgagtg ttgttccagt ttggaacaag 4080 agtccactat taaagaacgt ggactccaac gtcaaagggc gaaaaaccgt ctatcagggc 4140 gatggcccac tactccggga tcatatgaca agatgtgtat ccaccttaac ttaatgattt 4200 ttaccaaaat cattagggga ttcatcagtg ctcagggtca acgagaatta acattccgtc 4260 aggaaagctt atgatgatga tgtgcttaaa aacttactca atggctggtt atgcatatcg 4320 caatacatgc gaaaaaccta aaagagcttg ccgataaaaa aggccaattt attgctattt 4380 accgcggctt tttattgagc ttgaaagata aataaaatag ataggtttta tttgaagcta 4440 aatcttcttt atcgtaaaaa atgccctctt gggttatcaa gagggtcatt atatttcgcg 4500 gaataacatc atttggtgac gaaataacta agcacttgtc tcctgtttac tcccctgagc 4560 ttgaggggtt aacatgaagg tcatcgatag caggataata atacagtaaa acgctaaacc 4620 aataatccaa atccagccat cccaaattgg tagtgaatga ttataaataa cagcaaacag 4680 taatgggcca ataacaccgg ttgcattggt aaggctcacc aataatccct gtaaagcacc 4740 ttgctgatga ctctttgttt ggatagacat cactccctgt aatgcaggta aagcgatccc 4800 accaccagcc aataaaatta aaacagggaa aactaaccaa ccttcagata taaacgctaa 4860 aaaggcaaat gcactactat ctgcaataaa tccgagcagt actgccgttt tttcgcccat 4920 ttagtggcta ttcttcctgc cacaaaggct tggaatactg agtgtaaaag accaagaccc 4980 gtaatgaaaa gccaaccatc atgctattca tcatcacgat ttctgtaata gcaccacacc 5040 gtgctggatt ggctatcaat gcgctgaaat aataatcaac aaatggcatc gttaaataag 5100 tgatgtatac cgatcagctt ttgttccctt tagtgagggt taattgcgcg cttggcgtaa 5160 tcatggtcat agctgtttcc tgtgtgaaat tgttatccgc tcacaattcc acacaacata 5220 cgagccggaa gcataaagtg taaagcctgg ggtgcctaat gagtgagcta actcacatta 5280 attgcgttgc gctcactgcc cgctttccag tcgggaaacc tgtcgtgcca gctgcattaa 5340 tgaatcggcc aacgcgcggg gagaggcggt ttgcgtattg ggcgctcttc cgcttcctcg 5400 ctcactgact cgctgcgctc ggtcgttcgg ctgcggcgag cggtatcagc tcactcaaag 5460 gcggtaatac ggttatccac agaatcaggg gataacgcag gaaagaacat gtgagcaaaa 5520 ggccagcaaa aggccaggaa ccgtaaaaag gccgcgttgc tggcgttttt ccataggctc 5580 cgcccccctg acgagcatca caaaaatcga cgctcaagtc agaggtggcg aaacccgaca 5640 ggactataaa gataccaggc gtttccccct ggaagctccc tcgtgcgctc tcctgttccg 5700 accctgccgc ttaccggata cctgtccgcc tttctccctt cgggaagcgt ggcgctttct 5760 catagctcac gctgtaggta tctcagttcg gtgtaggtcg ttcgctccaa gctgggctgt 5820 gtgcacgaac cccccgttca gcccgaccgc tgcgccttat ccggtaacta tcgtcttgag 5880 tccaacccgg taagacacga cttatcgcca ctggcagcag ccactggtaa caggattagc 5940 agagcgaggt atgtaggcgg tgctacagag ttcttgaagt ggtggcctaa ctacggctac 6000 actagaagga cagtatttgg tatctgcgct ctgctgaagc cagttacctt cggaaaaaga 6060 gttggtagct cttgatccgg caaacaaacc accgctggta gcggtggttt ttttgtttgc 6120 aagcagcaga ttacgcgcag aaaaaaagga tctcaagaag atcctttgat cttttctacg 6180 gggtctgacg ctcagtggaa cgaaaactca cgttaaggga ttttggtcat gagattatca 6240 aaaaggatct tcacctagat ccttttaaat taaaaatgaa gttttaaatc aatctaaagt 6300 atatatgagt aaacttggtc tgacagttac caatgcttaa tcagtgaggc acctatctca 6360 gcgatctgtc tatttcgttc atccatagtt gcctgactcc ccgtcgtgta gataactacg 6420 atacgggagg gcttaccatc tggccccagt gctgcaatga taccgcgaga cccacgctca 6480 ccggctccag atttatcagc aataaaccag ccagccggaa gggccgagcg cagaagtggt 6540 cctgcaactt tatccgcctc catccagtct attaattgtt gccgggaagc tagagtaagt 6600 agttcgccag ttaatagttt gcgcaacgtt gttgccattg ctacaggcat cgtggtgtca 6660 cgctcgtcgt ttggtatggc ttcattcagc tccggttccc aacgatcaag gcgagttaca 6720 tgatccccca tgttgtgcaa aaaagcggtt agctccttcg gtcctccgat cgttgtcaga 6780 agtaagttgg ccgcagtgtt atcactcatg gttatggcag cactgcataa ttctcttact 6840 gtcatgccat ccgtaagatg cttttctgtg actggtgagt actcaaccaa gtcattctga 6900 gaatagtgta tgcggcgacc gagttgctct tgcccggcgt caatacggga taataccgcg 6960 ccacatagca gaactttaaa agtgctcatc attggaaaac gttcttcggg gcgaaaactc 7020 tcaaggatct taccgctgtt gagatccagt tcgatgtaac ccactcgtgc acccaactga 7080 tcttcagcat cttttacttt caccagcgtt tctgggtgag caaaaacagg aaggcaaaat 7140 gccgcaaaaa agggaataag ggcgacacgg aaatgttgaa tactcatact cttccttttt 7200 caatattatt gaagcattta tcagggttat tgtctcatga gcggatacat atttgaatgt 7260 atttagaaaa ataaacaaat aggggttccg cgcacatttc cccgaaaagt gccac 7315 57 7689 DNA ARTIFICIAL SEQUENCE Synthetic 57 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgtga acttgatatt 1800 ttacatgatt ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggaatac gatgcccatt gtacttgttg actggtctga tattcgtgag caaaaacgac 2100 ttatggtatt gcgagcttca gtcgcactac acggtcgttc tgttactctt tatgagaaag 2160 cgttcccgct ttcagagcaa tgttcaaaga aagctcatga ccaatttcta gccgaccttg 2220 cgagcattct accgagtaac accacaccgc tcattgtcag tgatgctggc tttaaagtgc 2280 catggtataa atccgttgag aagctgggtt ggtactggtt aagtcgagta agaggaaaag 2340 tacaatatgc agacctagga gcggaaaact ggaaacctat cagcaactta catgatatgt 2400 catctagtca ctcaaagact ttaggctata agaggctgac taaaagcaat ccaatctcat 2460 gccaaattct attgtataaa tctcgctcta aaggccgaaa aaatcagcgc tcgacacgga 2520 ctcattgtca ccacccgtca cctaaaatct actcagcgtc ggcaaaggag ccatgggttc 2580 tagcaactaa cttacctgtt gaaattcgaa cacccaaaca acttgttaat atctattcga 2640 agcgaatgca gattgaagaa accttccgag acttgaaaag tcctgcctac ggactaggcc 2700 tacgccatag ccgaacgagc agctcagagc gttttgatat catgctgcta atcgccctga 2760 tgcttcaact aacatgttgg cttgcgggcg ttcatgctca gaaacaaggt tgggacaagc 2820 acttccaggc taacacagtc agaaatcgaa acgtactctc aacagttcgc ttaggcatgg 2880 aagttttgcg gcattctggc tacacaataa caagggaaga cttactcgtg gctgcaaccc 2940 tactagctca aaatttattc acacatggtt acgctttggg gaaattatga taatgatcca 3000 gatcacttct ggctaataaa agatcagagc tctagagatc tgtgtgttgg ttttttgtgg 3060 atctgctgtg ccttctagtt gccagccatc tgttgtttgc ccctcccccg tgccttcctt 3120 gaccctggaa ggtgccactc ccactgtcct ttcctaataa aatgaggaaa ttgcatcgca 3180 ttgtctgagt aggtgtcatt ctattctggg gggtggggtg gggcagcaca gcaaggggga 3240 ggattgggaa gacaatagca ggcatgctgg ggatgcggtg ggctctatgg gtacctctct 3300 ctctctctct ctctctctct ctctctctct ctctcggtac ctctctctct ctctctctct 3360 ctctctctct ctctctctct cggtaccagg tgctgaagaa ttgacccggt gaccaaaggt 3420 gccttttatc atcactttaa aaataaaaaa caattactca gtgcctgtta taagcagcaa 3480 ttaattatga ttgatgccta catcacaaca aaaactgatt taacaaatgg ttggtctgcc 3540 ttagaaagta tatttgaaca ttatcttgat tatattattg ataataataa aaaccttatc 3600 cctatccaag aagtgatgcc tatcattggt tggaatgaac ttgaaaaaaa ttagccttga 3660 atacattact ggtaaggtaa acgccattgt cagcaaattg atccaagaga accaacttaa 3720 agctttcctg acggaatgtt aattctcgtt gaccctgagc actgatgaat cccctaatga 3780 ttttggtaaa aatcattaag ttaaggtgga tacacatctt gtcatatgat cccggtaatg 3840 tgagttagct cactcattag gcaccccagg ctttacactt tatgcttccg gctcgtatgt 3900 tgtgtggaat tgtgagcgga taacaatttc acacaggaaa cagctatgac catgattacg 3960 ccaagcgcgc aattaaccct cactaaaggg aacaaaagct ggagctccac cgcggtggcg 4020 gccgctctag aactagtgga tcccccgggc tgcaggaatt cgatatcaag cttatcgata 4080 ccgctgacct cgaggggggg cccggtaccc aattcgccct atagtgagtc gtattacgcg 4140 cgctcactgg ccgtcgtttt acaacgtcgt gactgggaaa accctggcgt tacccaactt 4200 aatcgccttg cagcacatcc ccctttcgcc agctggcgta atagcgaaga ggcccgcacc 4260 gatcgccctt cccaacagtt gcgcagcctg aatggcgaat ggaaattgta agcgttaata 4320 ttttgttaaa attcgcgtta aatttttgtt aaatcagctc attttttaac caataggccg 4380 aaatcggcaa aatcccttat aaatcaaaag aatagaccga gatagggttg agtgttgttc 4440 cagtttggaa caagagtcca ctattaaaga acgtggactc caacgtcaaa gggcgaaaaa 4500 ccgtctatca gggcgatggc ccactactcc gggatcatat gacaagatgt gtatccacct 4560 taacttaatg atttttacca aaatcattag gggattcatc agtgctcagg gtcaacgaga 4620 attaacattc cgtcaggaaa gcttatgatg atgatgtgct taaaaactta ctcaatggct 4680 ggttatgcat atcgcaatac atgcgaaaaa cctaaaagag cttgccgata aaaaaggcca 4740 atttattgct atttaccgcg gctttttatt gagcttgaaa gataaataaa atagataggt 4800 tttatttgaa gctaaatctt ctttatcgta aaaaatgccc tcttgggtta tcaagagggt 4860 cattatattt cgcggaataa catcatttgg tgacgaaata actaagcact tgtctcctgt 4920 ttactcccct gagcttgagg ggttaacatg aaggtcatcg atagcaggat aataatacag 4980 taaaacgcta aaccaataat ccaaatccag ccatcccaaa ttggtagtga atgattataa 5040 ataacagcaa acagtaatgg gccaataaca ccggttgcat tggtaaggct caccaataat 5100 ccctgtaaag caccttgctg atgactcttt gtttggatag acatcactcc ctgtaatgca 5160 ggtaaagcga tcccaccacc agccaataaa attaaaacag ggaaaactaa ccaaccttca 5220 gatataaacg ctaaaaaggc aaatgcacta ctatctgcaa taaatccgag cagtactgcc 5280 gttttttcgc ccatttagtg gctattcttc ctgccacaaa ggcttggaat actgagtgta 5340 aaagaccaag acccgtaatg aaaagccaac catcatgcta ttcatcatca cgatttctgt 5400 aatagcacca caccgtgctg gattggctat caatgcgctg aaataataat caacaaatgg 5460 catcgttaaa taagtgatgt ataccgatca gcttttgttc cctttagtga gggttaattg 5520 cgcgcttggc gtaatcatgg tcatagctgt ttcctgtgtg aaattgttat ccgctcacaa 5580 ttccacacaa catacgagcc ggaagcataa agtgtaaagc ctggggtgcc taatgagtga 5640 gctaactcac attaattgcg ttgcgctcac tgcccgcttt ccagtcggga aacctgtcgt 5700 gccagctgca ttaatgaatc ggccaacgcg cggggagagg cggtttgcgt attgggcgct 5760 cttccgcttc ctcgctcact gactcgctgc gctcggtcgt tcggctgcgg cgagcggtat 5820 cagctcactc aaaggcggta atacggttat ccacagaatc aggggataac gcaggaaaga 5880 acatgtgagc aaaaggccag caaaaggcca ggaaccgtaa aaaggccgcg ttgctggcgt 5940 ttttccatag gctccgcccc cctgacgagc atcacaaaaa tcgacgctca agtcagaggt 6000 ggcgaaaccc gacaggacta taaagatacc aggcgtttcc ccctggaagc tccctcgtgc 6060 gctctcctgt tccgaccctg ccgcttaccg gatacctgtc cgcctttctc ccttcgggaa 6120 gcgtggcgct ttctcatagc tcacgctgta ggtatctcag ttcggtgtag gtcgttcgct 6180 ccaagctggg ctgtgtgcac gaaccccccg ttcagcccga ccgctgcgcc ttatccggta 6240 actatcgtct tgagtccaac ccggtaagac acgacttatc gccactggca gcagccactg 6300 gtaacaggat tagcagagcg aggtatgtag gcggtgctac agagttcttg aagtggtggc 6360 ctaactacgg ctacactaga aggacagtat ttggtatctg cgctctgctg aagccagtta 6420 ccttcggaaa aagagttggt agctcttgat ccggcaaaca aaccaccgct ggtagcggtg 6480 gtttttttgt ttgcaagcag cagattacgc gcagaaaaaa aggatctcaa gaagatcctt 6540 tgatcttttc tacggggtct gacgctcagt ggaacgaaaa ctcacgttaa gggattttgg 6600 tcatgagatt atcaaaaagg atcttcacct agatcctttt aaattaaaaa tgaagtttta 6660 aatcaatcta aagtatatat gagtaaactt ggtctgacag ttaccaatgc ttaatcagtg 6720 aggcacctat ctcagcgatc tgtctatttc gttcatccat agttgcctga ctccccgtcg 6780 tgtagataac tacgatacgg gagggcttac catctggccc cagtgctgca atgataccgc 6840 gagacccacg ctcaccggct ccagatttat cagcaataaa ccagccagcc ggaagggccg 6900 agcgcagaag tggtcctgca actttatccg cctccatcca gtctattaat tgttgccggg 6960 aagctagagt aagtagttcg ccagttaata gtttgcgcaa cgttgttgcc attgctacag 7020 gcatcgtggt gtcacgctcg tcgtttggta tggcttcatt cagctccggt tcccaacgat 7080 caaggcgagt tacatgatcc cccatgttgt gcaaaaaagc ggttagctcc ttcggtcctc 7140 cgatcgttgt cagaagtaag ttggccgcag tgttatcact catggttatg gcagcactgc 7200 ataattctct tactgtcatg ccatccgtaa gatgcttttc tgtgactggt gagtactcaa 7260 ccaagtcatt ctgagaatag tgtatgcggc gaccgagttg ctcttgcccg gcgtcaatac 7320 gggataatac cgcgccacat agcagaactt taaaagtgct catcattgga aaacgttctt 7380 cggggcgaaa actctcaagg atcttaccgc tgttgagatc cagttcgatg taacccactc 7440 gtgcacccaa ctgatcttca gcatctttta ctttcaccag cgtttctggg tgagcaaaaa 7500 caggaaggca aaatgccgca aaaaagggaa taagggcgac acggaaatgt tgaatactca 7560 tactcttcct ttttcaatat tattgaagca tttatcaggg ttattgtctc atgagcggat 7620 acatatttga atgtatttag aaaaataaac aaataggggt tccgcgcaca tttccccgaa 7680 aagtgccac 7689 58 7 DNA ARTIFICIAL SEQUENCE Synthetic 58 accatgg 7 59 7 DNA ARTIFICIAL SEQUENCE Synthetic 59 accatgt 7 60 7 DNA ARTIFICIAL SEQUENCE Synthetic 60 aagatgt 7 61 7 DNA ARTIFICIAL SEQUENCE Synthetic 61 acgatga 7 62 7 DNA ARTIFICIAL SEQUENCE Synthetic 62 aagatgg 7 63 7 DNA ARTIFICIAL SEQUENCE Synthetic 63 gacatga 7 64 7 DNA ARTIFICIAL SEQUENCE Synthetic 64 accatga 7 65 7 DNA ARTIFICIAL SEQUENCE Synthetic 65 accatgt 7 66 315 DNA GALLUS SP. 66 tctgccattg ctgcttcctc tgcccttcct cgtcactctg aatgtggctt cttcgctact 60 gccacagcaa gaaataaaat ctcaacatct aaatgggttt cctgaggttt ttcaagagtc 120 gttaagcaca ttccttcccc agcacccctt gctgcaggcc agtgccaggc accaacttgg 180 ctactgctgc ccatgagaga aatccagttc aatattttcc aaagcaaaat ggattacata 240 tgccctagat cctgattaac aggcgtttgt attatctagt gctttcgctt cacccagatt 300 atcccattgc ctccc 315 67 361 DNA ARTIFICIAL SEQUENCE Synthetic 67 ggcgcctgga tccagatcac ttctggctaa taaaagatca gagctctaga gatctgtgtg 60 ttggtttttt gtggatctgc tgtgccttct agttgccagc catctgttgt ttgcccctcc 120 cccgtgcctt ccttgaccct ggaaggtgcc actcccactg tcctttccta ataaaatgag 180 gaaattgcat cgcattgtct gagtaggtgt cattctattc tggggggtgg ggtggggcag 240 cacagcaagg gggaggattg ggaagacaat agcaggcatg ctggggatgc ggtgggctct 300 atgggtacct ctctctctct ctctctctct ctctctctct ctctctctcg gtacctctct 360 c 361 68 350 DNA ARTIFICIAL SEQUENCE Synthetic 68 ggggatcgct ctagagcgat ccgggatctc gggaaaagcg ttggtgacca aaggtgcctt 60 ttatcatcac tttaaaaata aaaaacaatt actcagtgcc tgttataagc agcaattaat 120 tatgattgat gcctacatca caacaaaaac tgatttaaca aatggttggt ctgccttaga 180 aagtatattt gaacattatc ttgattatat tattgataat aataaaaacc ttatccctat 240 ccaagaagtg atgcctatca ttggttggaa tgaacttgaa aaaaattagc cttgaataca 300 ttactggtaa ggtaaacgcc attgtcagca aattgatcca agagaaccaa 350 69 908 DNA ARTIFICIAL SEQUENCE Synthetic 69 tgaatgtgtt cttgtgttat caatataaat cacagttagt gatgaagttg gctgcaagcc 60 tgcatcagtt cagctacttg gctgcatttt gtatttggtt ctgtaggaaa tgcaaaaggt 120 tctaggctga cctgcacttc tatccctctt gccttactgc tgagaatctc tgcaggtttt 180 aattgttcac attttgctcc catttacttt ggaagataaa atatttacag aatgcttatg 240 aaacctttgt tcatttaaaa atattcctgg tcagcgtgac cggagctgaa agaacacatt 300 gatcccgtga tttcaataaa tacatatgtt ccatatattg tttctcagta gcctcttaaa 360 tcatgtgcgt tggtgcacat atgaatacat gaatagcaaa ggtttatctg gattacgctc 420 tggcctgcag gaatggccat aaaccaaagc tgagggaaga gggagagtat agtcaatgta 480 gattatactg attgctgatt gggttattat cagctagata acaacttggg tcaggtgcca 540 ggtcaacata acctgggcaa aaccagtctc atctgtggca ggaccatgta ccagcagcca 600 gccgtgaccc aatctaggaa agcaagtagc acatcaattt taaatttatt gtaaatgccg 660 tagtagaagt gttttactgt gatacattga aacttctggt caatcagaaa aaggtttttt 720 atcagagatg ccaaggtatt atttgatttt ctttattcgc cgtgaagaga atttatgatt 780 gcaaaaagag gagtgtttac ataaactgat aaaaaacttg aggaattcag cagaaaacag 840 ccacgtgttc ctgaacattc ttccataaaa gtctcaccat gcctggcaga gccctattca 900 ccttcgct 908 70 901 DNA Gallus 70 gaggtcagaa tggtttcttt actgtttgtc aattctatta tttcaataca gaacaatagc 60 ttctataact gaaatatatt tgctattgta tattatgatt gtccctcgaa ccatgaacac 120 tcctccagct gaatttcaca attcctctgt catctgccag gccattaagt tattcatgga 180 agatctttga ggaacactgc aagttcatat cataaacaca tttgaaattg agtattgttt 240 tgcattgtat ggagctatgt tttgctgtat cctcagaaaa aaagtttgtt ataaagcatt 300 cacacccata aaaagataga tttaaatatt ccagctatag gaaagaaagt gcgtctgctc 360 ttcactctag tctcagttgg ctccttcaca tgcatgcttc tttatttctc ctattttgtc 420 aagaaaataa taggtcacgt cttgttctca cttatgtcct gcctagcatg gctcagatgc 480 acgttgtaga tacaagaagg atcaaatgaa acagacttct ggtctgttac tacaaccata 540 gtaataagca cactaactaa taattgctaa ttatgttttc catctctaag gttcccacat 600 ttttctgttt tcttaaagat cccattatct ggttgtaact gaagctcaat ggaacatgag 660 caatatttcc cagtcttctc tcccatccaa cagtcctgat ggattagcag aacaggcaga 720 aaacacattg ttacccagaa ttaaaaacta atatttgctc tccattcaat ccaaaatgga 780 cctattgaaa ctaaaatcta acccaatccc attaaatgat ttctatggcg tcaaaggtca 840 aacttctgaa gggaacctgt gggtgggtca caattcaggc tatatattcc ccagggctca 900 g 901 71 680 DNA GALLUS SP. 71 ccgggctgca gaaaaatgcc aggtggacta tgaactcaca tccaaaggag cttgacctga 60 tacctgattt tcttcaaact ggggaaacaa cacaatccca caaaacagct cagagagaaa 120 ccatcactga tggctacagc accaaggtat gcaatggcaa tccattcgac attcatctgt 180 gacctgagca aaatgattta tctctccatg aatggttgct tctttccctc atgaaaaggc 240 aatttccaca ctcacaatat gcaacaaaga caaacagaga acaattaatg tgctccttcc 300 taatgtcaaa attgtagtgg caaagaggag aacaaaatct caagttctga gtaggtttta 360 gtgattggat aagaggcttt gacctgtgag ctcacctgga cttcatatcc ttttggataa 420 aaagtgcttt tataactttc aggtctccga gtctttattc atgagactgt tggtttaggg 480 acagacccac aatgaaatgc ctggcatagg aaagggcagc agagccttag ctgacctttt 540 cttgggacaa gcattgtcaa acaatgtgtg acaaaactat ttgtactgct ttgcacagct 600 gtgctgggca gggcaatcca ttgccaccta tcccaggtaa ccttccaact gcaagaagat 660 tgttgcttac tctctctaga 680 72 72 DNA ARTIFICIAL SEQUENCE Synthetic 72 gtggatcaac atacagctag aaagctgtat tgcctttagc actcaagctc aaaagacaac 60 tcagagttca cc 72 73 62 DNA ARTIFICIAL SEQUENCE Synthetic 73 acatacagct agaaagctgt attgccttta gcactcaagc tcaaaagaca actcagagtt 60 ca 62 74 1158 DNA Gallus 74 atgggctcca tcggcgcagc aagcatggaa ttttgttttg atgtattcaa ggagctcaaa 60 gtccaccatg ccaatgagaa catcttctac tgccccattg ccatcatgtc agctctagcc 120 atggtatacc tgggtgcaaa agacagcacc aggacacaga taaataaggt tgttcgcttt 180 gataaacttc caggattcgg agacagtatt gaagctcagt gtggcacatc tgtaaacgtt 240 cactcttcac ttagagacat cctcaaccaa atcaccaaac caaatgatgt ttattcgttc 300 agccttgcca gtagacttta tgctgaagag agatacccaa tcctgccaga atacttgcag 360 tgtgtgaagg aactgtatag aggaggcttg gaacctatca actttcaaac agctgcagat 420 caagccagag agctcatcaa ttcctgggta gaaagtcaga caaatggaat tatcagaaat 480 gtccttcagc caagctccgt ggattctcaa actgcaatgg ttctggttaa tgccattgtc 540 ttcaaaggac tgtgggagaa aacatttaag gatgaagaca cacaagcaat gcctttcaga 600 gtgactgagc aagaaagcaa acctgtgcag atgatgtacc agattggttt atttagagtg 660 gcatcaatgg cttctgagaa aatgaagatc ctggagcttc catttgccag tgggacaatg 720 agcatgttgg tgctgttgcc tgatgaagtc tcaggccttg agcagcttga gagtataatc 780 aactttgaaa aactgactga atggaccagt tctaatgtta tggaagagag gaagatcaaa 840 gtgtacttac ctcgcatgaa gatggaggaa aaatacaacc tcacatctgt cttaatggct 900 atgggcatta ctgacgtgtt tagctcttca gccaatctgt ctggcatctc ctcagcagag 960 agcctgaaga tatctcaagc tgtccatgca gcacatgcag aaatcaatga agcaggcaga 1020 gaggtggtag ggtcagcaga ggctggagtg gatgctgcaa gcgtctctga agaatttagg 1080 gctgaccatc cattcctctt ctgtatcaag cacatcgcaa ccaacgccgt tctcttcttt 1140 ggcagatgtg tttcccct 1158 75 51 DNA Gallus 75 atgggctcca tcggcgcagc aagcatggaa ttttgttttg atgtattcaa g 51 76 105 DNA Gallus 76 atgggctcca tcggcgcagc aagcatggaa ttttgttttg atgtattcaa ggagctcaaa 60 gtccaccatg ccaatgagaa catcttctac tgccccattg ccatc 105 77 63 DNA ARTIFICIAL SEQUENCE Synthetic 77 atgaggggga tcatactggc attagtgctc acccttgtag gcagccagaa gtttgacatt 60 ggt 63 78 13 PRT ARTIFICIAL SEQUENCE Synthetic 78 Lys Tyr Lys Lys Ala Leu Lys Lys Leu Ala Lys Leu Leu 1 5 10 79 39 DNA ARTIFICIAL SEQUENCE Synthetic 79 aaatacaaaa aagcactgaa aaaactggca aaactgctg 39 80 260 DNA ARTIFICIAL SEQUENCE Synthetic 80 tttgtgaacc aacacctgtg cggctcacac ctggtggaag ctctctacct agtgtgcggg 60 gaacgaggct tcttctacac acccaagacc cgccgggagg cagaggacct gcaggtgggg 120 caggtggagc tgggcggggg ccctggtgca ggcagcctgc agcccttggc cctggagggg 180 tccctgcaga agcgtggcat tgtggaacaa tgctgtacca gcatctgctc cctctaccag 240 ctggagaact ctgcaactag 260 81 4 PRT ARTIFICIAL SEQUENCE Synthetic 81 Gly Pro Gly Gly 1 82 12 PRT ARTIFICIAL SEQUENCE Synthetic 82 Gly Pro Gly Gly Gly Pro Gly Gly Gly Pro Gly Gly 1 5 10 83 15 PRT ARTIFICIAL SEQUENCE Synthetic 83 Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 1 5 10 15 84 20 PRT ARTIFICIAL SEQUENCE Synthetic 84 Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly 1 5 10 15 Gly Gly Gly Ser 20 85 5 PRT ARTIFICIAL SEQUENCE Synthetic 85 Pro Ala Asp Asp Ala 1 5 86 29 PRT ARTIFICIAL SEQUENCE Synthetic 86 Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro 1 5 10 15 Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp 20 25 87 16 PRT ARTIFICIAL SEQUENCE Synthetic 87 Ala Thr Thr Cys Ile Leu Lys Gly Ser Cys Gly Trp Ile Gly Leu Leu 1 5 10 15 88 30 PRT ARTIFICIAL SEQUENCE Synthetic 88 Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Thr Thr Cys Ile Leu Lys 1 5 10 15 Gly Ser Cys Gly Trp Ile Gly Leu Leu Asp Asp Asp Asp Lys 20 25 30 89 5 PRT ARTIFICIAL SEQUENCE Synthetic 89 Asp Asp Asp Asp Lys 1 5 90 50 PRT ARTIFICIAL SEQUENCE Synthetic 90 Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro 1 5 10 15 Ala Asp Asp Ala Pro Ala Asp Asp Ala Pro Ala Asp Asp Ala Thr Thr 20 25 30 Cys Ile Leu Lys Gly Ser Cys Gly Trp Ile Gly Leu Leu Asp Asp Asp 35 40 45 Asp Lys 50 91 48 DNA ARTIFICIAL SEQUENCE Synthetic 91 atctcgagac catgtgtgaa cttgatattt tacatgattc tctttacc 48 92 36 DNA ARTIFICIAL SEQUENCE Synthetic 92 gattgatcat tatcataatt tccccaaagc gtaacc 36 93 6 DNA ARTIFICIAL SEQUENCE Synthetic 93 ctcgag 6 94 6 DNA ARTIFICIAL SEQUENCE Synthetic 94 tgatca 6 95 22 DNA ARTIFICIAL SEQUENCE Synthetic 95 ttgccggcat cagattggct at 22 96 34 DNA ARTIFICIAL SEQUENCE Synthetic 96 agaggtcacc gggtcaattc ttcagcacct ggta 34 97 11973 DNA ARTIFICIAL SEQUENCE Synthetic 97 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgtga acttgatatt 1800 ttacatgatt ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg ataatgatcc 3000 agatcacttc tggctaataa aagatcagag ctctagagat ctgtgtgttg gttttttgtg 3060 gatctgctgt gccttctagt tgccagccat ctgttgtttg cccctccccc gtgccttcct 3120 tgaccctgga aggtgccact cccactgtcc tttcctaata aaatgaggaa attgcatcgc 3180 attgtctgag taggtgtcat tctattctgg ggggtggggt ggggcagcac agcaaggggg 3240 aggattggga agacaatagc aggcatgctg gggatgcggt gggctctatg ggtacctctc 3300 tctctctctc tctctctctc tctctctctc tctctcggta cctctctctc tctctctctc 3360 tctctctctc tctctctctc tcggtaccag gtgctgaaga attgacccgg tgaccaaagg 3420 tgccttttat catcacttta aaaataaaaa acaattactc agtgcctgtt ataagcagca 3480 attaattatg attgatgcct acatcacaac aaaaactgat ttaacaaatg gttggtctgc 3540 cttagaaagt atatttgaac attatcttga ttatattatt gataataata aaaaccttat 3600 ccctatccaa gaagtgatgc ctatcattgg ttggaatgaa cttgaaaaaa attagccttg 3660 aatacattac tggtaaggta aacgccattg tcagcaaatt gatccaagag aaccaactta 3720 aagctttcct gacggaatgt taattctcgt tgaccctgag cactgatgaa tcccctaatg 3780 attttggtaa aaatcattaa gttaaggtgg atacacatct tgtcatatga tcccggtaat 3840 gtgagttagc tcactcatta ggcaccccag gctttacact ttatgcttcc ggctcgtatg 3900 ttgtgtggaa ttgtgagcgg ataacaattt cacacaggaa acagctatga ccatgattac 3960 gccaagcgcg caattaaccc tcactaaagg gaacaaaagc tggagctcca ccgcggtggc 4020 ggccgctcta gaactagtgg atcccccggg ctgcaggaat tcgatatcaa gcttatcgat 4080 accgctgacc tcgagcatca gattggctat tggccattgc atacgttgta tccatatcat 4140 aatatgtaca tttatattgg ctcatgtcca acattaccgc catgttgaca ttgattattg 4200 actagttatt aatagtaatc aattacgggg tcattagttc atagcccata tatggagttc 4260 cgcgttacat aacttacggt aaatggcccg cctggctgac cgcccaacga cccccgccca 4320 ttgacgtcaa taatgacgta tgttcccata gtaacgccaa tagggacttt ccattgacgt 4380 caatgggtgg agtatttacg gtaaactgcc cacttggcag tacatcaagt gtatcatatg 4440 tcaagtacgc cccctattga cgtcaatgac ggtaaatggc ccgcctggca ttatgcccag 4500 tacatgacct tatgggactt tcctacttgg cagtacatct acgtattagt catcgctatt 4560 accatggtga tgcggttttg gcagtacatc aatgggcgtg gatagcggtt tgactcacgg 4620 ggatttccaa gtcttcaccc cattgacgtc aatgggagtt tgttttggca ccaaaatcaa 4680 cgggactttc caaaatgtcg taacaactcc gccccattga cgcaaatggg cggtaggcgt 4740 gtacggtggg aggtctatat aagcagagct cgtttagtga accgtcagat cgcctggaga 4800 cgccatccac gctgttttga cctccataga agacaccggg accgatccag cctccgcggc 4860 cgggaacggt gcattggaac gcggattccc cgtgccaaga gtgacgtaag taccgcctat 4920 agactctata ggcacacccc tttggctctt atgcatgcta tactgttttt ggcttggggc 4980 ctatacaccc ccgcttcctt atgctatagg tgatggtata gcttagccta taggtgtggg 5040 ttattgacca ttattgacca ctcccctatt ggtgacgata ctttccatta ctaatccata 5100 acatggctct ttgccacaac tatctctatt ggctatatgc caatactctg tccttcagag 5160 actgacacgg actctgtatt tttacaggat ggggtcccat ttattattta caaattcaca 5220 tatacaacaa cgccgtcccc cgtgcccgca gtttttatta aacatagcgt gggatctcca 5280 cgcgaatctc gggtacgtgt tccggacatg ggctcttctc cggtagcggc ggagcttcca 5340 catccgagcc ctggtcccat gcctccagcg gctcatggtc gctcggcagc tccttgctcc 5400 taacagtgga ggccagactt aggcacagca caatgcccac caccaccagt gtgccgcaca 5460 aggccgtggc ggtagggtat gtgtctgaaa atgagcgtgg agattgggct cgcacggctg 5520 acgcagatgg aagacttaag gcagcggcag aagaagatgc aggcagctga gttgttgtat 5580 tctgataaga gtcagaggta actcccgttg cggtgctgtt aacggtggag ggcagtgtag 5640 tctgagcagt actcgttgct gccgcgcgcg ccaccagaca taatagctga cagactaaca 5700 gactgttcct ttccatgggt cttttctgca gtcaccgtcg gatcaatcat tcatctcgtg 5760 acttcttcgt gtgtggtgtt tacctatata tctaaattta atatttcgtt tattaaaatt 5820 taatatattt cgacgatgaa tttctcaagg atatttttct tcgtgttcgc tttggttctg 5880 gctttgtcaa cagtttcggc tgcgccagag ccgaaaggta cccaggtgca gctgcaggag 5940 tcggggggag gcttggtaaa gccggggggg tcccttagag tctcctgtgc agcctctgga 6000 ttcactttca gaaacgcctg gatgagctgg gtccgccagg ctccagggaa ggggctggag 6060 tgggtcggcc gtattaaaag caaaattgat ggtgggacaa cagactatgc tgcacccgtg 6120 aaaggcagat tcaccatctc aagagatgat tcaaaaaaca cgttatatct gcaaatgaat 6180 agcctgaaag ccgaggacac agccgtatat tactgtacca cggggattat gataacattt 6240 gggggagtta tccctccccc gaattggggc cagggaaccc tggtcaccgt ctcctcagcc 6300 tccaccaagg gcccatcggt cttccccctg gcaccctcct ccaagagcac ctctgggggc 6360 acagcggccc tgggctgcct ggtcaaggac tacttccccg aaccggtgac ggtgtcgtgg 6420 aactcaggcg ccctgaccag cggcgtgcac acctttccgg ctgtcctaca gtcctcagga 6480 ctctacttcc ttagcaacgt ggtgaccgtg ccctccagca gcttgggcac ccagacctac 6540 atctgcaacg tgaatcacaa gcccagcaac accaaggtgg acaagaaagt tgagcccaaa 6600 tcttgtgaca aaactcacac atgcccaccg tgcccagcac ctgaactcct ggggggaccg 6660 tcagtcttcc tcttcccccc aaaacccaag gacaccctca tgatctcccg gacccctgag 6720 gtcacatgcg tggtggtgga cgtgagccac gaagaccctg aggtcaagtt caactggtac 6780 gtggacggcg tggaggtgca taatgccaag acaaagccgc gggaggagca gtacaacagc 6840 acgtaccgtg tggtcagcgt cctcaccgtc ctgcaccagg actggctgaa tggcaaggag 6900 tacaagtgca aggtctccaa caaagccctc ccagccccca tcgagaaaac catctccaaa 6960 gccaaagggc agccccgaga accacaggtg tacaccctgc ccccatcccg ggatgagctg 7020 accaagaacc aggtcagcct gacctgcctg gtcaaaggct tctatcccag cgacatcgcc 7080 gtggagtggg agagcaatgg gcagccggag aacaactaca agaccacgcc tcccgtgctg 7140 gactccgacg gctccttctt cctctacagc aagctcaccg tggacaagag caggtggcag 7200 caggggaacg tcttctcatg ctccgtgatg catgaggctc tgcacaacca ctacacgcag 7260 aagagcctct ccctgtctcc gggtaaagcg ccagagccga aaaagctttc ctatgagctg 7320 acacagccac cctcggtgtc agtgtcccca ggacaaacgg ccaggatcac ctgctctgga 7380 gatgcattgc cagaaaaata tgtttattgg taccagcaga agtcaggcca ggcccctgtg 7440 gtggtcatct atgaggacag caaacgaccc tccgggatcc ctgagagatt ctctggctcc 7500 agctcaggga caatggccac cttgactatc agtggggccc aggtggaaga tgaaggtgac 7560 tactactgtt actcaactga cagcagtggt tatcataggg aggtgttcag cggagggacc 7620 aagctgaccg tcctaggtca gcccaaggct gccccctcgg tcactctgtt cccaccctcc 7680 tctgaggagc ttcaagccaa caaggccaca ctggtgtgtc tcataagtga ctcctacccg 7740 ggagccgtga cagtggcctg gaaggcagat agcagccccg tcaaggcggg agtggagacc 7800 accacaccct ccaaacaaag caacaacaag tacgcggcca gcagctacct gagcctgacg 7860 cttgagcagt ggaagtccca caaaagctac agctgccagg tcacgcatga agggagcacc 7920 gtggagaaga cagtggcccc tgcagaatgt tcaccgcgga gggagggaag ggcccttttt 7980 gaagggggag gaaacttcgc gccatgactc ctctcgtgcc ccccgcacgg aacactgatg 8040 tgcagagggc cctctgccat tgctgcttcc tctgcccttc ctcgtcactc tgaatgtggc 8100 ttctttgcta ctgccacagc aagaaataaa atctcaacat ctaaatgggt ttcctgagat 8160 ttttcaagag tcgttaagca cattccttcc ccagcacccc ttgctgcagg ccagtgccag 8220 gcaccaactt ggctactgct gcccatgaga gaaatccagt tcaatatttt ccaaagcaaa 8280 atggattaca tatgccctag atcctgatta acaggtgttt tgtattatct gtgctttcgc 8340 ttcacccaca ttatcccatt gcctcccctc gactcgaggg ggggcccggt acccaattcg 8400 ccctatagtg agtcgtatta cgcgcgctca ctggccgtcg ttttacaacg tcgtgactgg 8460 gaaaaccctg gcgttaccca acttaatcgc cttgcagcac atcccccttt cgccagctgg 8520 cgtaatagcg aagaggcccg caccgatcgc ccttcccaac agttgcgcag cctgaatggc 8580 gaatggaaat tgtaagcgtt aatattttgt taaaattcgc gttaaatttt tgttaaatca 8640 gctcattttt taaccaatag gccgaaatcg gcaaaatccc ttataaatca aaagaataga 8700 ccgagatagg gttgagtgtt gttccagttt ggaacaagag tccactatta aagaacgtgg 8760 actccaacgt caaagggcga aaaaccgtct atcagggcga tggcccacta ctccgggatc 8820 atatgacaag atgtgtatcc accttaactt aatgattttt accaaaatca ttaggggatt 8880 catcagtgct cagggtcaac gagaattaac attccgtcag gaaagcttat gatgatgatg 8940 tgcttaaaaa cttactcaat ggctggttat gcatatcgca atacatgcga aaaacctaaa 9000 agagcttgcc gataaaaaag gccaatttat tgctatttac cgcggctttt tattgagctt 9060 gaaagataaa taaaatagat aggttttatt tgaagctaaa tcttctttat cgtaaaaaat 9120 gccctcttgg gttatcaaga gggtcattat atttcgcgga ataacatcat ttggtgacga 9180 aataactaag cacttgtctc ctgtttactc ccctgagctt gaggggttaa catgaaggtc 9240 atcgatagca ggataataat acagtaaaac gctaaaccaa taatccaaat ccagccatcc 9300 caaattggta gtgaatgatt ataaataaca gcaaacagta atgggccaat aacaccggtt 9360 gcattggtaa ggctcaccaa taatccctgt aaagcacctt gctgatgact ctttgtttgg 9420 atagacatca ctccctgtaa tgcaggtaaa gcgatcccac caccagccaa taaaattaaa 9480 acagggaaaa ctaaccaacc ttcagatata aacgctaaaa aggcaaatgc actactatct 9540 gcaataaatc cgagcagtac tgccgttttt tcgcccattt agtggctatt cttcctgcca 9600 caaaggcttg gaatactgag tgtaaaagac caagacccgt aatgaaaagc caaccatcat 9660 gctattcatc atcacgattt ctgtaatagc accacaccgt gctggattgg ctatcaatgc 9720 gctgaaataa taatcaacaa atggcatcgt taaataagtg atgtataccg atcagctttt 9780 gttcccttta gtgagggtta attgcgcgct tggcgtaatc atggtcatag ctgtttcctg 9840 tgtgaaattg ttatccgctc acaattccac acaacatacg agccggaagc ataaagtgta 9900 aagcctgggg tgcctaatga gtgagctaac tcacattaat tgcgttgcgc tcactgcccg 9960 ctttccagtc gggaaacctg tcgtgccagc tgcattaatg aatcggccaa cgcgcgggga 10020 gaggcggttt gcgtattggg cgctcttccg cttcctcgct cactgactcg ctgcgctcgg 10080 tcgttcggct gcggcgagcg gtatcagctc actcaaaggc ggtaatacgg ttatccacag 10140 aatcagggga taacgcagga aagaacatgt gagcaaaagg ccagcaaaag gccaggaacc 10200 gtaaaaaggc cgcgttgctg gcgtttttcc ataggctccg cccccctgac gagcatcaca 10260 aaaatcgacg ctcaagtcag aggtggcgaa acccgacagg actataaaga taccaggcgt 10320 ttccccctgg aagctccctc gtgcgctctc ctgttccgac cctgccgctt accggatacc 10380 tgtccgcctt tctcccttcg ggaagcgtgg cgctttctca tagctcacgc tgtaggtatc 10440 tcagttcggt gtaggtcgtt cgctccaagc tgggctgtgt gcacgaaccc cccgttcagc 10500 ccgaccgctg cgccttatcc ggtaactatc gtcttgagtc caacccggta agacacgact 10560 tatcgccact ggcagcagcc actggtaaca ggattagcag agcgaggtat gtaggcggtg 10620 ctacagagtt cttgaagtgg tggcctaact acggctacac tagaaggaca gtatttggta 10680 tctgcgctct gctgaagcca gttaccttcg gaaaaagagt tggtagctct tgatccggca 10740 aacaaaccac cgctggtagc ggtggttttt ttgtttgcaa gcagcagatt acgcgcagaa 10800 aaaaaggatc tcaagaagat cctttgatct tttctacggg gtctgacgct cagtggaacg 10860 aaaactcacg ttaagggatt ttggtcatga gattatcaaa aaggatcttc acctagatcc 10920 ttttaaatta aaaatgaagt tttaaatcaa tctaaagtat atatgagtaa acttggtctg 10980 acagttacca atgcttaatc agtgaggcac ctatctcagc gatctgtcta tttcgttcat 11040 ccatagttgc ctgactcccc gtcgtgtaga taactacgat acgggagggc ttaccatctg 11100 gccccagtgc tgcaatgata ccgcgagacc cacgctcacc ggctccagat ttatcagcaa 11160 taaaccagcc agccggaagg gccgagcgca gaagtggtcc tgcaacttta tccgcctcca 11220 tccagtctat taattgttgc cgggaagcta gagtaagtag ttcgccagtt aatagtttgc 11280 gcaacgttgt tgccattgct acaggcatcg tggtgtcacg ctcgtcgttt ggtatggctt 11340 cattcagctc cggttcccaa cgatcaaggc gagttacatg atcccccatg ttgtgcaaaa 11400 aagcggttag ctccttcggt cctccgatcg ttgtcagaag taagttggcc gcagtgttat 11460 cactcatggt tatggcagca ctgcataatt ctcttactgt catgccatcc gtaagatgct 11520 tttctgtgac tggtgagtac tcaaccaagt cattctgaga atagtgtatg cggcgaccga 11580 gttgctcttg cccggcgtca atacgggata ataccgcgcc acatagcaga actttaaaag 11640 tgctcatcat tggaaaacgt tcttcggggc gaaaactctc aaggatctta ccgctgttga 11700 gatccagttc gatgtaaccc actcgtgcac ccaactgatc ttcagcatct tttactttca 11760 ccagcgtttc tgggtgagca aaaacaggaa ggcaaaatgc cgcaaaaaag ggaataaggg 11820 cgacacggaa atgttgaata ctcatactct tcctttttca atattattga agcatttatc 11880 agggttattg tctcatgagc ggatacatat ttgaatgtat ttagaaaaat aaacaaatag 11940 gggttccgcg cacatttccc cgaaaagtgc cac 11973 98 11964 DNA ARTIFICIAL SEQUENCE Synthetic 98 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgcga actcgatatt 1800 ttacacgact ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg aggggatcgc 3000 tctagagcga tccgggatct cgggaaaagc gttggtgacc aaaggtgcct tttatcatca 3060 ctttaaaaat aaaaaacaat tactcagtgc ctgttataag cagcaattaa ttatgattga 3120 tgcctacatc acaacaaaaa ctgatttaac aaatggttgg tctgccttag aaagtatatt 3180 tgaacattat cttgattata ttattgataa taataaaaac cttatcccta tccaagaagt 3240 gatgcctatc attggttgga atgaacttga aaaaaattag ccttgaatac attactggta 3300 aggtaaacgc cattgtcagc aaattgatcc aagagaacca acttaaagct ttcctgacgg 3360 aatgttaatt ctcgttgacc ctgagcactg atgaatcccc taatgatttt ggtaaaaatc 3420 attaagttaa ggtggataca catcttgtca tatgatcccg gtaatgtgag ttagctcact 3480 cattaggcac cccaggcttt acactttatg cttccggctc gtatgttgtg tggaattgtg 3540 agcggataac aatttcacac aggaaacagc tatgaccatg attacgccaa gcgcgcaatt 3600 aaccctcact aaagggaaca aaagctggag ctccaccgcg gtggcggccg ctctagaact 3660 agtggatccc ccgggctgca ggaattcgat atcaagctta tcgataccgc tgacctcgag 3720 ctgcagaaaa atgccaggtg gactatgaac tcacatccaa aggagcttga cctgatacct 3780 gattttcttc aaacagggga aacaacacaa tcccacaaaa cagctcagag agaaaccatc 3840 actgatggct acagcaccaa ggtatgcaat ggcaatccat tcgacattca tctgtgacct 3900 gagcaaaatg atttctctct ccatgaatgg ttgcttcttt ccctcatgaa aaggcaattt 3960 ccacactcac aatatgcgac aaagacaaac agagaacaat taatgtgctc cttcctaatg 4020 tcaaaattgt agtggcaaag aggagaacaa aatctcaagt tctgagtagg ttttagtgat 4080 tggataagag gctttgacct gtgagctcac ctggacttca tatccttttg gataaaaagt 4140 gcttttataa ctttcaggtc tccgagtctt tattcatgag actgttggtt tagggacaga 4200 cccacaatga aatgcctggc ataggaaagg gcagcagagc cttagctgac cttttcttgg 4260 gacaagcatt gtcaaacaat gtgtgacaaa actatttgta ctgctttgca cagctgtgct 4320 gggcagggcg atccattgcc acctatccca ggtaaccttc caactgcaag aagattgttg 4380 cttactctct ctagaaagct tctgcagact gacatgcatt tcataggtag agataacatt 4440 tactgggaag cacatctatc atcacaaaaa gcaggcaaga ttttcagact ttcttagtgg 4500 ctgaaataga agcaaaagac gtaattaaaa acaaaatgaa acaaaaaaaa tcagttgata 4560 cctgtggtgt agacatccag caaaaaaata ttatttgcac taccatcttg tcttaagtcc 4620 tcagacttag caaggagaat gtagatttcc acagtatata tgttttcaca aaaggaagga 4680 gagaaacaaa agaaaatggc actgactaaa cttcagctag tggtatagga aagtaattct 4740 gcttaacaga gattgcagtg atctctatgt atgtcctgaa gaattatgtt gtactttttt 4800 cccccatttt taaatcaaac agtgctttac agaggtcaga atggtttctt tactgtttgt 4860 caattctatt atttcaatac agaacaatag cttctataac tgaaatatat ttgctattgt 4920 atattatgat tgtccctcga accatgaaca ctcctccagc tgaatttcac aattcctctg 4980 tcatctgcca ggccattaag ttattcatgg aagatctttg aggaacactg caagttcata 5040 tcataaacac atttgaaatt gagtattggt ttgcattgta tggagctatg ttttgctgta 5100 tcctcagaaa aaaagtttgt tataaagcat tcacacccat aaaaagatag atttaaatat 5160 tccagctata ggaaagaaag tgcgtctgct cttcactcta gtctcagttg gctccttcac 5220 atgcatgctt ctttatttct cctattttgt caagaaaata ataggtcacg tcttgttctc 5280 acttatgtcc tgcctagcat ggctcagatg cacgttgtag atacaagaag gatcaaatga 5340 aacagacttc tggtctgtta cctacaacca tagtaataag cacactaact aataattgct 5400 aattatgttt tccatctcta aggttcccat atttttctgt tttcttaaag atcccattat 5460 ctggttgtaa ctgaagctca atggaacatg agcaatattt cccagtcttc tctcccatcc 5520 aacagtcctg atggattagc agaacaggca gaaaacacat tgttacccag aattaaaaac 5580 taatatttgc tctccattca atccaaaatg gacctattga aactaaaatc taacccaatc 5640 ccattaaatg atttctatgg tgtcaaaggt caaacttctg aagggaacct gtgggtgggt 5700 cacaattcag gctatatatt ccccagggct cagccagtgg atcaatcatt catctcgtga 5760 cttcttcgtg tgtggtgttt acctatatat ctaaatttaa tatttcgttt attaaaattt 5820 aatatatttc gacgatgaat ttctcaagga tatttttctt cgtgttcgct ttggttctgg 5880 ctttgtcaac agtttcggct gcgccagagc cgaaaggtac ccaggtgcag ctgcaggagt 5940 cggggggagg cttggtaaag ccgggggggt cccttagagt ctcctgtgca gcctctggat 6000 tcactttcag aaacgcctgg atgagctggg tccgccaggc tccagggaag gggctggagt 6060 gggtcggccg tattaaaagc aaaattgatg gtgggacaac agactatgct gcacccgtga 6120 aaggcagatt caccatctca agagatgatt caaaaaacac gttatatctg caaatgaata 6180 gcctgaaagc cgaggacaca gccgtatatt actgtaccac ggggattatg ataacatttg 6240 ggggagttat ccctcccccg aattggggcc agggaaccct ggtcaccgtc tcctcagcct 6300 ccaccaaggg cccatcggtc ttccccctgg caccctcctc caagagcacc tctgggggca 6360 cagcggccct gggctgcctg gtcaaggact acttccccga accggtgacg gtgtcgtgga 6420 actcaggcgc cctgaccagc ggcgtgcaca cctttccggc tgtcctacag tcctcaggac 6480 tctacttcct tagcaacgtg gtgaccgtgc cctccagcag cttgggcacc cagacctaca 6540 tctgcaacgt gaatcacaag cccagcaaca ccaaggtgga caagaaagtt gagcccaaat 6600 cttgtgacaa aactcacaca tgcccaccgt gcccagcacc tgaactcctg gggggaccgt 6660 cagtcttcct cttcccccca aaacccaagg acaccctcat gatctcccgg acccctgagg 6720 tcacatgcgt ggtggtggac gtgagccacg aagaccctga ggtcaagttc aactggtacg 6780 tggacggcgt ggaggtgcat aatgccaaga caaagccgcg ggaggagcag tacaacagca 6840 cgtaccgtgt ggtcagcgtc ctcaccgtcc tgcaccagga ctggctgaat ggcaaggagt 6900 acaagtgcaa ggtctccaac aaagccctcc cagcccccat cgagaaaacc atctccaaag 6960 ccaaagggca gccccgagaa ccacaggtgt acaccctgcc cccatcccgg gatgagctga 7020 ccaagaacca ggtcagcctg acctgcctgg tcaaaggctt ctatcccagc gacatcgccg 7080 tggagtggga gagcaatggg cagccggaga acaactacaa gaccacgcct cccgtgctgg 7140 actccgacgg ctccttcttc ctctacagca agctcaccgt ggacaagagc aggtggcagc 7200 aggggaacgt cttctcatgc tccgtgatgc atgaggctct gcacaaccac tacacgcaga 7260 agagcctctc cctgtctccg ggtaaagcgc cagagccgaa gctttcctat gagctgacac 7320 agccaccctc ggtgtcagtg tccccaggac aaacggccag gatcacctgc tctggagatg 7380 cattgccaga aaaatatgtt tattggtacc agcagaagtc aggccaggcc cctgtggtgg 7440 tcatctatga ggacagcaaa cgaccctccg ggatccctga gagattctct ggctccagct 7500 cagggacaat ggccaccttg actatcagtg gggcccaggt ggaagatgaa ggtgactact 7560 actgttactc aactgacagc agtggttatc atagggaggt gttcagcgga gggaccaagc 7620 tgaccgtcct aggtcagccc aaggctgccc cctcggtcac tctgttccca ccctcctctg 7680 aggagcttca agccaacaag gccacactgg tgtgtctcat aagtgactcc tacccgggag 7740 ccgtgacagt ggcctggaag gcagatagca gccccgtcaa ggcgggagtg gagaccacca 7800 caccctccaa acaaagcaac aacaagtacg cggccagcag ctacctgagc ctgacgcttg 7860 agcagtggaa gtcccacaaa agctacagct gccaggtcac gcatgaaggg agcaccgtgg 7920 agaagacagt ggcccctgca gaatgttcac cgcggaggga gggaagggcc ctttttgaag 7980 ggggaggaaa cttcgcgcca tgactcctct cgtgcccccc gcacggaaca ctgatgtgca 8040 gagggccctc tgccattgct gcttcctctg cccttcctcg tcactctgaa tgtggcttct 8100 ttgctactgc cacagcaaga aataaaatct caacatctaa atgggtttcc tgagattttt 8160 caagagtcgt taagcacatt ccttccccag caccccttgc tgcaggccag tgccaggcac 8220 caacttggct actgctgccc atgagagaaa tccagttcaa tattttccaa agcaaaatgg 8280 attacatatg ccctagatcc tgattaacag gtgttttgta ttatctgtgc tttcgcttca 8340 cccacattat cccattgcct cccctcgagg gggggcccgg tacccaattc gccctatagt 8400 gagtcgtatt acgcgcgctc actggccgtc gttttacaac gtcgtgactg ggaaaaccct 8460 ggcgttaccc aacttaatcg ccttgcagca catccccctt tcgccagctg gcgtaatagc 8520 gaagaggccc gcaccgatcg cccttcccaa cagttgcgca gcctgaatgg cgaatggaaa 8580 ttgtaagcgt taatattttg ttaaaattcg cgttaaattt ttgttaaatc agctcatttt 8640 ttaaccaata ggccgaaatc ggcaaaatcc cttataaatc aaaagaatag accgagatag 8700 ggttgagtgt tgttccagtt tggaacaaga gtccactatt aaagaacgtg gactccaacg 8760 tcaaagggcg aaaaaccgtc tatcagggcg atggcccact actccgggat catatgacaa 8820 gatgtgtatc caccttaact taatgatttt taccaaaatc attaggggat tcatcagtgc 8880 tcagggtcaa cgagaattaa cattccgtca ggaaagctta tgatgatgat gtgcttaaaa 8940 acttactcaa tggctggtta tgcatatcgc aatacatgcg aaaaacctaa aagagcttgc 9000 cgataaaaaa ggccaattta ttgctattta ccgcggcttt ttattgagct tgaaagataa 9060 ataaaataga taggttttat ttgaagctaa atcttcttta tcgtaaaaaa tgccctcttg 9120 ggttatcaag agggtcatta tatttcgcgg aataacatca tttggtgacg aaataactaa 9180 gcacttgtct cctgtttact cccctgagct tgaggggtta acatgaaggt catcgatagc 9240 aggataataa tacagtaaaa cgctaaacca ataatccaaa tccagccatc ccaaattggt 9300 agtgaatgat tataaataac agcaaacagt aatgggccaa taacaccggt tgcattggta 9360 aggctcacca ataatccctg taaagcacct tgctgatgac tctttgtttg gatagacatc 9420 actccctgta atgcaggtaa agcgatccca ccaccagcca ataaaattaa aacagggaaa 9480 actaaccaac cttcagatat aaacgctaaa aaggcaaatg cactactatc tgcaataaat 9540 ccgagcagta ctgccgtttt ttcgcccatt tagtggctat tcttcctgcc acaaaggctt 9600 ggaatactga gtgtaaaaga ccaagacccg taatgaaaag ccaaccatca tgctattcat 9660 catcacgatt tctgtaatag caccacaccg tgctggattg gctatcaatg cgctgaaata 9720 ataatcaaca aatggcatcg ttaaataagt gatgtatacc gatcagcttt tgttcccttt 9780 agtgagggtt aattgcgcgc ttggcgtaat catggtcata gctgtttcct gtgtgaaatt 9840 gttatccgct cacaattcca cacaacatac gagccggaag cataaagtgt aaagcctggg 9900 gtgcctaatg agtgagctaa ctcacattaa ttgcgttgcg ctcactgccc gctttccagt 9960 cgggaaacct gtcgtgccag ctgcattaat gaatcggcca acgcgcgggg agaggcggtt 10020 tgcgtattgg gcgctcttcc gcttcctcgc tcactgactc gctgcgctcg gtcgttcggc 10080 tgcggcgagc ggtatcagct cactcaaagg cggtaatacg gttatccaca gaatcagggg 10140 ataacgcagg aaagaacatg tgagcaaaag gccagcaaaa ggccaggaac cgtaaaaagg 10200 ccgcgttgct ggcgtttttc cataggctcc gcccccctga cgagcatcac aaaaatcgac 10260 gctcaagtca gaggtggcga aacccgacag gactataaag ataccaggcg tttccccctg 10320 gaagctccct cgtgcgctct cctgttccga ccctgccgct taccggatac ctgtccgcct 10380 ttctcccttc gggaagcgtg gcgctttctc atagctcacg ctgtaggtat ctcagttcgg 10440 tgtaggtcgt tcgctccaag ctgggctgtg tgcacgaacc ccccgttcag cccgaccgct 10500 gcgccttatc cggtaactat cgtcttgagt ccaacccggt aagacacgac ttatcgccac 10560 tggcagcagc cactggtaac aggattagca gagcgaggta tgtaggcggt gctacagagt 10620 tcttgaagtg gtggcctaac tacggctaca ctagaaggac agtatttggt atctgcgctc 10680 tgctgaagcc agttaccttc ggaaaaagag ttggtagctc ttgatccggc aaacaaacca 10740 ccgctggtag cggtggtttt tttgtttgca agcagcagat tacgcgcaga aaaaaaggat 10800 ctcaagaaga tcctttgatc ttttctacgg ggtctgacgc tcagtggaac gaaaactcac 10860 gttaagggat tttggtcatg agattatcaa aaaggatctt cacctagatc cttttaaatt 10920 aaaaatgaag ttttaaatca atctaaagta tatatgagta aacttggtct gacagttacc 10980 aatgcttaat cagtgaggca cctatctcag cgatctgtct atttcgttca tccatagttg 11040 cctgactccc cgtcgtgtag ataactacga tacgggaggg cttaccatct ggccccagtg 11100 ctgcaatgat accgcgagac ccacgctcac cggctccaga tttatcagca ataaaccagc 11160 cagccggaag ggccgagcgc agaagtggtc ctgcaacttt atccgcctcc atccagtcta 11220 ttaattgttg ccgggaagct agagtaagta gttcgccagt taatagtttg cgcaacgttg 11280 ttgccattgc tacaggcatc gtggtgtcac gctcgtcgtt tggtatggct tcattcagct 11340 ccggttccca acgatcaagg cgagttacat gatcccccat gttgtgcaaa aaagcggtta 11400 gctccttcgg tcctccgatc gttgtcagaa gtaagttggc cgcagtgtta tcactcatgg 11460 ttatggcagc actgcataat tctcttactg tcatgccatc cgtaagatgc ttttctgtga 11520 ctggtgagta ctcaaccaag tcattctgag aatagtgtat gcggcgaccg agttgctctt 11580 gcccggcgtc aatacgggat aataccgcgc cacatagcag aactttaaaa gtgctcatca 11640 ttggaaaacg ttcttcgggg cgaaaactct caaggatctt accgctgttg agatccagtt 11700 cgatgtaacc cactcgtgca cccaactgat cttcagcatc ttttactttc accagcgttt 11760 ctgggtgagc aaaaacagga aggcaaaatg ccgcaaaaaa gggaataagg gcgacacgga 11820 aatgttgaat actcatactc ttcctttttc aatattattg aagcatttat cagggttatt 11880 gtctcatgag cggatacata tttgaatgta tttagaaaaa taaacaaata ggggttccgc 11940 gcacatttcc ccgaaaagtg ccac 11964 99 11967 DNA ARTIFICIAL SEQUENCE Synthetic 99 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgcga actcgatatt 1800 ttacacgact ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg aggggatcgc 3000 tctagagcga tccgggatct cgggaaaagc gttggtgacc aaaggtgcct tttatcatca 3060 ctttaaaaat aaaaaacaat tactcagtgc ctgttataag cagcaattaa ttatgattga 3120 tgcctacatc acaacaaaaa ctgatttaac aaatggttgg tctgccttag aaagtatatt 3180 tgaacattat cttgattata ttattgataa taataaaaac cttatcccta tccaagaagt 3240 gatgcctatc attggttgga atgaacttga aaaaaattag ccttgaatac attactggta 3300 aggtaaacgc cattgtcagc aaattgatcc aagagaacca acttaaagct ttcctgacgg 3360 aatgttaatt ctcgttgacc ctgagcactg atgaatcccc taatgatttt ggtaaaaatc 3420 attaagttaa ggtggataca catcttgtca tatgatcccg gtaatgtgag ttagctcact 3480 cattaggcac cccaggcttt acactttatg cttccggctc gtatgttgtg tggaattgtg 3540 agcggataac aatttcacac aggaaacagc tatgaccatg attacgccaa gcgcgcaatt 3600 aaccctcact aaagggaaca aaagctggag ctccaccgcg gtggcggccg ctctagaact 3660 agtggatccc ccgggctgca ggaattcgat atcaagctta tcgataccgc tgacctcgag 3720 ctgcagaaaa atgccaggtg gactatgaac tcacatccaa aggagcttga cctgatacct 3780 gattttcttc aaacagggga aacaacacaa tcccacaaaa cagctcagag agaaaccatc 3840 actgatggct acagcaccaa ggtatgcaat ggcaatccat tcgacattca tctgtgacct 3900 gagcaaaatg atttctctct ccatgaatgg ttgcttcttt ccctcatgaa aaggcaattt 3960 ccacactcac aatatgcgac aaagacaaac agagaacaat taatgtgctc cttcctaatg 4020 tcaaaattgt agtggcaaag aggagaacaa aatctcaagt tctgagtagg ttttagtgat 4080 tggataagag gctttgacct gtgagctcac ctggacttca tatccttttg gataaaaagt 4140 gcttttataa ctttcaggtc tccgagtctt tattcatgag actgttggtt tagggacaga 4200 cccacaatga aatgcctggc ataggaaagg gcagcagagc cttagctgac cttttcttgg 4260 gacaagcatt gtcaaacaat gtgtgacaaa actatttgta ctgctttgca cagctgtgct 4320 gggcagggcg atccattgcc acctatccca ggtaaccttc caactgcaag aagattgttg 4380 cttactctct ctagaaagct tctgcagact gacatgcatt tcataggtag agataacatt 4440 tactgggaag cacatctatc atcacaaaaa gcaggcaaga ttttcagact ttcttagtgg 4500 ctgaaataga agcaaaagac gtaattaaaa acaaaatgaa acaaaaaaaa tcagttgata 4560 cctgtggtgt agacatccag caaaaaaata ttatttgcac taccatcttg tcttaagtcc 4620 tcagacttag caaggagaat gtagatttcc acagtatata tgttttcaca aaaggaagga 4680 gagaaacaaa agaaaatggc actgactaaa cttcagctag tggtatagga aagtaattct 4740 gcttaacaga gattgcagtg atctctatgt atgtcctgaa gaattatgtt gtactttttt 4800 cccccatttt taaatcaaac agtgctttac agaggtcaga atggtttctt tactgtttgt 4860 caattctatt atttcaatac agaacaatag cttctataac tgaaatatat ttgctattgt 4920 atattatgat tgtccctcga accatgaaca ctcctccagc tgaatttcac aattcctctg 4980 tcatctgcca ggccattaag ttattcatgg aagatctttg aggaacactg caagttcata 5040 tcataaacac atttgaaatt gagtattggt ttgcattgta tggagctatg ttttgctgta 5100 tcctcagaaa aaaagtttgt tataaagcat tcacacccat aaaaagatag atttaaatat 5160 tccagctata ggaaagaaag tgcgtctgct cttcactcta gtctcagttg gctccttcac 5220 atgcatgctt ctttatttct cctattttgt caagaaaata ataggtcacg tcttgttctc 5280 acttatgtcc tgcctagcat ggctcagatg cacgttgtag atacaagaag gatcaaatga 5340 aacagacttc tggtctgtta cctacaacca tagtaataag cacactaact aataattgct 5400 aattatgttt tccatctcta aggttcccat atttttctgt tttcttaaag atcccattat 5460 ctggttgtaa ctgaagctca atggaacatg agcaatattt cccagtcttc tctcccatcc 5520 aacagtcctg atggattagc agaacaggca gaaaacacat tgttacccag aattaaaaac 5580 taatatttgc tctccattca atccaaaatg gacctattga aactaaaatc taacccaatc 5640 ccattaaatg atttctatgg tgtcaaaggt caaacttctg aagggaacct gtgggtgggt 5700 cacaattcag gctatatatt ccccagggct cagccagtgg atcaatcatt catctcgtga 5760 cttcttcgtg tgtggtgttt acctatatat ctaaatttaa tatttcgttt attaaaattt 5820 aatatatttc gacgatgaat ttctcaagga tatttttctt cgtgttcgct ttggttctgg 5880 ctttgtcaac agtttcggct gcgccagagc cgaaaggtac ccaggtgcag ctgcaggagt 5940 cggggggagg cttggtaaag ccgggggggt cccttagagt ctcctgtgca gcctctggat 6000 tcactttcag aaacgcctgg atgagctggg tccgccaggc tccagggaag gggctggagt 6060 gggtcggccg tattaaaagc aaaattgatg gtgggacaac agactatgct gcacccgtga 6120 aaggcagatt caccatctca agagatgatt caaaaaacac gttatatctg caaatgaata 6180 gcctgaaagc cgaggacaca gccgtatatt actgtaccac ggggattatg ataacatttg 6240 ggggagttat ccctcccccg aattggggcc agggaaccct ggtcaccgtc tcctcagcct 6300 ccaccaaggg cccatcggtc ttccccctgg caccctcctc caagagcacc tctgggggca 6360 cagcggccct gggctgcctg gtcaaggact acttccccga accggtgacg gtgtcgtgga 6420 actcaggcgc cctgaccagc ggcgtgcaca cctttccggc tgtcctacag tcctcaggac 6480 tctacttcct tagcaacgtg gtgaccgtgc cctccagcag cttgggcacc cagacctaca 6540 tctgcaacgt gaatcacaag cccagcaaca ccaaggtgga caagaaagtt gagcccaaat 6600 cttgtgacaa aactcacaca tgcccaccgt gcccagcacc tgaactcctg gggggaccgt 6660 cagtcttcct cttcccccca aaacccaagg acaccctcat gatctcccgg acccctgagg 6720 tcacatgcgt ggtggtggac gtgagccacg aagaccctga ggtcaagttc aactggtacg 6780 tggacggcgt ggaggtgcat aatgccaaga caaagccgcg ggaggagcag tacaacagca 6840 cgtaccgtgt ggtcagcgtc ctcaccgtcc tgcaccagga ctggctgaat ggcaaggagt 6900 acaagtgcaa ggtctccaac aaagccctcc cagcccccat cgagaaaacc atctccaaag 6960 ccaaagggca gccccgagaa ccacaggtgt acaccctgcc cccatcccgg gatgagctga 7020 ccaagaacca ggtcagcctg acctgcctgg tcaaaggctt ctatcccagc gacatcgccg 7080 tggagtggga gagcaatggg cagccggaga acaactacaa gaccacgcct cccgtgctgg 7140 actccgacgg ctccttcttc ctctacagca agctcaccgt ggacaagagc aggtggcagc 7200 aggggaacgt cttctcatgc tccgtgatgc atgaggctct gcacaaccac tacacgcaga 7260 agagcctctc cctgtctccg ggtaaagcgc cagagccgaa aaagctttcc tatgagctga 7320 cacagccacc ctcggtgtca gtgtccccag gacaaacggc caggatcacc tgctctggag 7380 atgcattgcc agaaaaatat gtttattggt accagcagaa gtcaggccag gcccctgtgg 7440 tggtcatcta tgaggacagc aaacgaccct ccgggatccc tgagagattc tctggctcca 7500 gctcagggac aatggccacc ttgactatca gtggggccca ggtggaagat gaaggtgact 7560 actactgtta ctcaactgac agcagtggtt atcataggga ggtgttcagc ggagggacca 7620 agctgaccgt cctaggtcag cccaaggctg ccccctcggt cactctgttc ccaccctcct 7680 ctgaggagct tcaagccaac aaggccacac tggtgtgtct cataagtgac tcctacccgg 7740 gagccgtgac agtggcctgg aaggcagata gcagccccgt caaggcggga gtggagacca 7800 ccacaccctc caaacaaagc aacaacaagt acgcggccag cagctacctg agcctgacgc 7860 ttgagcagtg gaagtcccac aaaagctaca gctgccaggt cacgcatgaa gggagcaccg 7920 tggagaagac agtggcccct gcagaatgtt caccgcggag ggagggaagg gccctttttg 7980 aagggggagg aaacttcgcg ccatgactcc tctcgtgccc cccgcacgga acactgatgt 8040 gcagagggcc ctctgccatt gctgcttcct ctgcccttcc tcgtcactct gaatgtggct 8100 tctttgctac tgccacagca agaaataaaa tctcaacatc taaatgggtt tcctgagatt 8160 tttcaagagt cgttaagcac attccttccc cagcacccct tgctgcaggc cagtgccagg 8220 caccaacttg gctactgctg cccatgagag aaatccagtt caatattttc caaagcaaaa 8280 tggattacat atgccctaga tcctgattaa caggtgtttt gtattatctg tgctttcgct 8340 tcacccacat tatcccattg cctcccctcg agggggggcc cggtacccaa ttcgccctat 8400 agtgagtcgt attacgcgcg ctcactggcc gtcgttttac aacgtcgtga ctgggaaaac 8460 cctggcgtta cccaacttaa tcgccttgca gcacatcccc ctttcgccag ctggcgtaat 8520 agcgaagagg cccgcaccga tcgcccttcc caacagttgc gcagcctgaa tggcgaatgg 8580 aaattgtaag cgttaatatt ttgttaaaat tcgcgttaaa tttttgttaa atcagctcat 8640 tttttaacca ataggccgaa atcggcaaaa tcccttataa atcaaaagaa tagaccgaga 8700 tagggttgag tgttgttcca gtttggaaca agagtccact attaaagaac gtggactcca 8760 acgtcaaagg gcgaaaaacc gtctatcagg gcgatggccc actactccgg gatcatatga 8820 caagatgtgt atccacctta acttaatgat ttttaccaaa atcattaggg gattcatcag 8880 tgctcagggt caacgagaat taacattccg tcaggaaagc ttatgatgat gatgtgctta 8940 aaaacttact caatggctgg ttatgcatat cgcaatacat gcgaaaaacc taaaagagct 9000 tgccgataaa aaaggccaat ttattgctat ttaccgcggc tttttattga gcttgaaaga 9060 taaataaaat agataggttt tatttgaagc taaatcttct ttatcgtaaa aaatgccctc 9120 ttgggttatc aagagggtca ttatatttcg cggaataaca tcatttggtg acgaaataac 9180 taagcacttg tctcctgttt actcccctga gcttgagggg ttaacatgaa ggtcatcgat 9240 agcaggataa taatacagta aaacgctaaa ccaataatcc aaatccagcc atcccaaatt 9300 ggtagtgaat gattataaat aacagcaaac agtaatgggc caataacacc ggttgcattg 9360 gtaaggctca ccaataatcc ctgtaaagca ccttgctgat gactctttgt ttggatagac 9420 atcactccct gtaatgcagg taaagcgatc ccaccaccag ccaataaaat taaaacaggg 9480 aaaactaacc aaccttcaga tataaacgct aaaaaggcaa atgcactact atctgcaata 9540 aatccgagca gtactgccgt tttttcgccc atttagtggc tattcttcct gccacaaagg 9600 cttggaatac tgagtgtaaa agaccaagac ccgtaatgaa aagccaacca tcatgctatt 9660 catcatcacg atttctgtaa tagcaccaca ccgtgctgga ttggctatca atgcgctgaa 9720 ataataatca acaaatggca tcgttaaata agtgatgtat accgatcagc ttttgttccc 9780 tttagtgagg gttaattgcg cgcttggcgt aatcatggtc atagctgttt cctgtgtgaa 9840 attgttatcc gctcacaatt ccacacaaca tacgagccgg aagcataaag tgtaaagcct 9900 ggggtgccta atgagtgagc taactcacat taattgcgtt gcgctcactg cccgctttcc 9960 agtcgggaaa cctgtcgtgc cagctgcatt aatgaatcgg ccaacgcgcg gggagaggcg 10020 gtttgcgtat tgggcgctct tccgcttcct cgctcactga ctcgctgcgc tcggtcgttc 10080 ggctgcggcg agcggtatca gctcactcaa aggcggtaat acggttatcc acagaatcag 10140 gggataacgc aggaaagaac atgtgagcaa aaggccagca aaaggccagg aaccgtaaaa 10200 aggccgcgtt gctggcgttt ttccataggc tccgcccccc tgacgagcat cacaaaaatc 10260 gacgctcaag tcagaggtgg cgaaacccga caggactata aagataccag gcgtttcccc 10320 ctggaagctc cctcgtgcgc tctcctgttc cgaccctgcc gcttaccgga tacctgtccg 10380 cctttctccc ttcgggaagc gtggcgcttt ctcatagctc acgctgtagg tatctcagtt 10440 cggtgtaggt cgttcgctcc aagctgggct gtgtgcacga accccccgtt cagcccgacc 10500 gctgcgcctt atccggtaac tatcgtcttg agtccaaccc ggtaagacac gacttatcgc 10560 cactggcagc agccactggt aacaggatta gcagagcgag gtatgtaggc ggtgctacag 10620 agttcttgaa gtggtggcct aactacggct acactagaag gacagtattt ggtatctgcg 10680 ctctgctgaa gccagttacc ttcggaaaaa gagttggtag ctcttgatcc ggcaaacaaa 10740 ccaccgctgg tagcggtggt ttttttgttt gcaagcagca gattacgcgc agaaaaaaag 10800 gatctcaaga agatcctttg atcttttcta cggggtctga cgctcagtgg aacgaaaact 10860 cacgttaagg gattttggtc atgagattat caaaaaggat cttcacctag atccttttaa 10920 attaaaaatg aagttttaaa tcaatctaaa gtatatatga gtaaacttgg tctgacagtt 10980 accaatgctt aatcagtgag gcacctatct cagcgatctg tctatttcgt tcatccatag 11040 ttgcctgact ccccgtcgtg tagataacta cgatacggga gggcttacca tctggcccca 11100 gtgctgcaat gataccgcga gacccacgct caccggctcc agatttatca gcaataaacc 11160 agccagccgg aagggccgag cgcagaagtg gtcctgcaac tttatccgcc tccatccagt 11220 ctattaattg ttgccgggaa gctagagtaa gtagttcgcc agttaatagt ttgcgcaacg 11280 ttgttgccat tgctacaggc atcgtggtgt cacgctcgtc gtttggtatg gcttcattca 11340 gctccggttc ccaacgatca aggcgagtta catgatcccc catgttgtgc aaaaaagcgg 11400 ttagctcctt cggtcctccg atcgttgtca gaagtaagtt ggccgcagtg ttatcactca 11460 tggttatggc agcactgcat aattctctta ctgtcatgcc atccgtaaga tgcttttctg 11520 tgactggtga gtactcaacc aagtcattct gagaatagtg tatgcggcga ccgagttgct 11580 cttgcccggc gtcaatacgg gataataccg cgccacatag cagaacttta aaagtgctca 11640 tcattggaaa acgttcttcg gggcgaaaac tctcaaggat cttaccgctg ttgagatcca 11700 gttcgatgta acccactcgt gcacccaact gatcttcagc atcttttact ttcaccagcg 11760 tttctgggtg agcaaaaaca ggaaggcaaa atgccgcaaa aaagggaata agggcgacac 11820 ggaaatgttg aatactcata ctcttccttt ttcaatatta ttgaagcatt tatcagggtt 11880 attgtctcat gagcggatac atatttgaat gtatttagaa aaataaacaa ataggggttc 11940 cgcgcacatt tccccgaaaa gtgccac 11967 100 11590 DNA ARTIFICIAL SEQUENCE Synthetic 100 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgcga actcgatatt 1800 ttacacgact ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg aggggatcgc 3000 tctagagcga tccgggatct cgggaaaagc gttggtgacc aaaggtgcct tttatcatca 3060 ctttaaaaat aaaaaacaat tactcagtgc ctgttataag cagcaattaa ttatgattga 3120 tgcctacatc acaacaaaaa ctgatttaac aaatggttgg tctgccttag aaagtatatt 3180 tgaacattat cttgattata ttattgataa taataaaaac cttatcccta tccaagaagt 3240 gatgcctatc attggttgga atgaacttga aaaaaattag ccttgaatac attactggta 3300 aggtaaacgc cattgtcagc aaattgatcc aagagaacca acttaaagct ttcctgacgg 3360 aatgttaatt ctcgttgacc ctgagcactg atgaatcccc taatgatttt ggtaaaaatc 3420 attaagttaa ggtggataca catcttgtca tatgatcccg gtaatgtgag ttagctcact 3480 cattaggcac cccaggcttt acactttatg cttccggctc gtatgttgtg tggaattgtg 3540 agcggataac aatttcacac aggaaacagc tatgaccatg attacgccaa gcgcgcaatt 3600 aaccctcact aaagggaaca aaagctggag ctccaccgcg gtggcggccg ctctagaact 3660 agtggatccc ccgggctgca ggaattcgat atcaagctta tcgataccgc tgacctcgag 3720 catcagattg gctattggcc attgcatacg ttgtatccat atcataatat gtacatttat 3780 attggctcat gtccaacatt accgccatgt tgacattgat tattgactag ttattaatag 3840 taatcaatta cggggtcatt agttcatagc ccatatatgg agttccgcgt tacataactt 3900 acggtaaatg gcccgcctgg ctgaccgccc aacgaccccc gcccattgac gtcaataatg 3960 acgtatgttc ccatagtaac gccaataggg actttccatt gacgtcaatg ggtggagtat 4020 ttacggtaaa ctgcccactt ggcagtacat caagtgtatc atatgtcaag tacgccccct 4080 attgacgtca atgacggtaa atggcccgcc tggcattatg cccagtacat gaccttatgg 4140 gactttccta cttggcagta catctacgta ttagtcatcg ctattaccat ggtgatgcgg 4200 ttttggcagt acatcaatgg gcgtggatag cggtttgact cacggggatt tccaagtctt 4260 caccccattg acgtcaatgg gagtttgttt tggcaccaaa atcaacggga ctttccaaaa 4320 tgtcgtaaca actccgcccc attgacgcaa atgggcggta ggcgtgtacg gtgggaggtc 4380 tatataagca gagctcgttt agtgaaccgt cagatcgcct ggagacgcca tccacgctgt 4440 tttgacctcc atagaagaca ccgggaccga tccagcctcc gcggccggga acggtgcatt 4500 ggaacgcgga ttccccgtgc caagagtgac gtaagtaccg cctatagact ctataggcac 4560 acccctttgg ctcttatgca tgctatactg tttttggctt ggggcctata cacccccgct 4620 tccttatgct ataggtgatg gtatagctta gcctataggt gtgggttatt gaccattatt 4680 gaccactccc ctattggtga cgatactttc cattactaat ccataacatg gctctttgcc 4740 acaactatct ctattggcta tatgccaata ctctgtcctt cagagactga cacggactct 4800 gtatttttac aggatggggt cccatttatt atttacaaat tcacatatac aacaacgccg 4860 tcccccgtgc ccgcagtttt tattaaacat agcgtgggat ctccacgcga atctcgggta 4920 cgtgttccgg acatgggctc ttctccggta gcggcggagc ttccacatcc gagccctggt 4980 cccatgcctc cagcggctca tggtcgctcg gcagctcctt gctcctaaca gtggaggcca 5040 gacttaggca cagcacaatg cccaccacca ccagtgtgcc gcacaaggcc gtggcggtag 5100 ggtatgtgtc tgaaaatgag cgtggagatt gggctcgcac ggctgacgca gatggaagac 5160 ttaaggcagc ggcagaagaa gatgcaggca gctgagttgt tgtattctga taagagtcag 5220 aggtaactcc cgttgcggtg ctgttaacgg tggagggcag tgtagtctga gcagtactcg 5280 ttgctgccgc gcgcgccacc agacataata gctgacagac taacagactg ttcctttcca 5340 tgggtctttt ctgcagtcac cgtcggatca atcattcatc tcgtgacttc ttcgtgtgtg 5400 gtgtttacct atatatctaa atttaatatt tcgtttatta aaatttaata tatttcgacg 5460 atgaatttct caaggatatt tttcttcgtg ttcgctttgg ttctggcttt gtcaacagtt 5520 tcggctgcgc cagagccgaa aggtacccag gtgcagctgc aggagtcggg gggaggcttg 5580 gtaaagccgg gggggtccct tagagtctcc tgtgcagcct ctggattcac tttcagaaac 5640 gcctggatga gctgggtccg ccaggctcca gggaaggggc tggagtgggt cggccgtatt 5700 aaaagcaaaa ttgatggtgg gacaacagac tatgctgcac ccgtgaaagg cagattcacc 5760 atctcaagag atgattcaaa aaacacgtta tatctgcaaa tgaatagcct gaaagccgag 5820 gacacagccg tatattactg taccacgggg attatgataa catttggggg agttatccct 5880 cccccgaatt ggggccaggg aaccctggtc accgtctcct cagcctccac caagggccca 5940 tcggtcttcc ccctggcacc ctcctccaag agcacctctg ggggcacagc ggccctgggc 6000 tgcctggtca aggactactt ccccgaaccg gtgacggtgt cgtggaactc aggcgccctg 6060 accagcggcg tgcacacctt tccggctgtc ctacagtcct caggactcta cttccttagc 6120 aacgtggtga ccgtgccctc cagcagcttg ggcacccaga cctacatctg caacgtgaat 6180 cacaagccca gcaacaccaa ggtggacaag aaagttgagc ccaaatcttg tgacaaaact 6240 cacacatgcc caccgtgccc agcacctgaa ctcctggggg gaccgtcagt cttcctcttc 6300 cccccaaaac ccaaggacac cctcatgatc tcccggaccc ctgaggtcac atgcgtggtg 6360 gtggacgtga gccacgaaga ccctgaggtc aagttcaact ggtacgtgga cggcgtggag 6420 gtgcataatg ccaagacaaa gccgcgggag gagcagtaca acagcacgta ccgtgtggtc 6480 agcgtcctca ccgtcctgca ccaggactgg ctgaatggca aggagtacaa gtgcaaggtc 6540 tccaacaaag ccctcccagc ccccatcgag aaaaccatct ccaaagccaa agggcagccc 6600 cgagaaccac aggtgtacac cctgccccca tcccgggatg agctgaccaa gaaccaggtc 6660 agcctgacct gcctggtcaa aggcttctat cccagcgaca tcgccgtgga gtgggagagc 6720 aatgggcagc cggagaacaa ctacaagacc acgcctcccg tgctggactc cgacggctcc 6780 ttcttcctct acagcaagct caccgtggac aagagcaggt ggcagcaggg gaacgtcttc 6840 tcatgctccg tgatgcatga ggctctgcac aaccactaca cgcagaagag cctctccctg 6900 tctccgggta aagcgccaga gccgaagctt tcctatgagc tgacacagcc accctcggtg 6960 tcagtgtccc caggacaaac ggccaggatc acctgctctg gagatgcatt gccagaaaaa 7020 tatgtttatt ggtaccagca gaagtcaggc caggcccctg tggtggtcat ctatgaggac 7080 agcaaacgac cctccgggat ccctgagaga ttctctggct ccagctcagg gacaatggcc 7140 accttgacta tcagtggggc ccaggtggaa gatgaaggtg actactactg ttactcaact 7200 gacagcagtg gttatcatag ggaggtgttc agcggaggga ccaagctgac cgtcctaggt 7260 cagcccaagg ctgccccctc ggtcactctg ttcccaccct cctctgagga gcttcaagcc 7320 aacaaggcca cactggtgtg tctcataagt gactcctacc cgggagccgt gacagtggcc 7380 tggaaggcag atagcagccc cgtcaaggcg ggagtggaga ccaccacacc ctccaaacaa 7440 agcaacaaca agtacgcggc cagcagctac ctgagcctga cgcttgagca gtggaagtcc 7500 cacaaaagct acagctgcca ggtcacgcat gaagggagca ccgtggagaa gacagtggcc 7560 cctgcagaat gttcaccgcg gagggaggga agggcccttt ttgaaggggg aggaaacttc 7620 gcgccatgac tcctctcgtg ccccccgcac ggaacactga tgtgcagagg gccctctgcc 7680 attgctgctt cctctgccct tcctcgtcac tctgaatgtg gcttctttgc tactgccaca 7740 gcaagaaata aaatctcaac atctaaatgg gtttcctgag atttttcaag agtcgttaag 7800 cacattcctt ccccagcacc ccttgctgca ggccagtgcc aggcaccaac ttggctactg 7860 ctgcccatga gagaaatcca gttcaatatt ttccaaagca aaatggatta catatgccct 7920 agatcctgat taacaggtgt tttgtattat ctgtgctttc gcttcaccca cattatccca 7980 ttgcctcccc tcgagggggg gcccggtacc caattcgccc tatagtgagt cgtattacgc 8040 gcgctcactg gccgtcgttt tacaacgtcg tgactgggaa aaccctggcg ttacccaact 8100 taatcgcctt gcagcacatc cccctttcgc cagctggcgt aatagcgaag aggcccgcac 8160 cgatcgccct tcccaacagt tgcgcagcct gaatggcgaa tggaaattgt aagcgttaat 8220 attttgttaa aattcgcgtt aaatttttgt taaatcagct cattttttaa ccaataggcc 8280 gaaatcggca aaatccctta taaatcaaaa gaatagaccg agatagggtt gagtgttgtt 8340 ccagtttgga acaagagtcc actattaaag aacgtggact ccaacgtcaa agggcgaaaa 8400 accgtctatc agggcgatgg cccactactc cgggatcata tgacaagatg tgtatccacc 8460 ttaacttaat gatttttacc aaaatcatta ggggattcat cagtgctcag ggtcaacgag 8520 aattaacatt ccgtcaggaa agcttatgat gatgatgtgc ttaaaaactt actcaatggc 8580 tggttatgca tatcgcaata catgcgaaaa acctaaaaga gcttgccgat aaaaaaggcc 8640 aatttattgc tatttaccgc ggctttttat tgagcttgaa agataaataa aatagatagg 8700 ttttatttga agctaaatct tctttatcgt aaaaaatgcc ctcttgggtt atcaagaggg 8760 tcattatatt tcgcggaata acatcatttg gtgacgaaat aactaagcac ttgtctcctg 8820 tttactcccc tgagcttgag gggttaacat gaaggtcatc gatagcagga taataataca 8880 gtaaaacgct aaaccaataa tccaaatcca gccatcccaa attggtagtg aatgattata 8940 aataacagca aacagtaatg ggccaataac accggttgca ttggtaaggc tcaccaataa 9000 tccctgtaaa gcaccttgct gatgactctt tgtttggata gacatcactc cctgtaatgc 9060 aggtaaagcg atcccaccac cagccaataa aattaaaaca gggaaaacta accaaccttc 9120 agatataaac gctaaaaagg caaatgcact actatctgca ataaatccga gcagtactgc 9180 cgttttttcg cccatttagt ggctattctt cctgccacaa aggcttggaa tactgagtgt 9240 aaaagaccaa gacccgtaat gaaaagccaa ccatcatgct attcatcatc acgatttctg 9300 taatagcacc acaccgtgct ggattggcta tcaatgcgct gaaataataa tcaacaaatg 9360 gcatcgttaa ataagtgatg tataccgatc agcttttgtt ccctttagtg agggttaatt 9420 gcgcgcttgg cgtaatcatg gtcatagctg tttcctgtgt gaaattgtta tccgctcaca 9480 attccacaca acatacgagc cggaagcata aagtgtaaag cctggggtgc ctaatgagtg 9540 agctaactca cattaattgc gttgcgctca ctgcccgctt tccagtcggg aaacctgtcg 9600 tgccagctgc attaatgaat cggccaacgc gcggggagag gcggtttgcg tattgggcgc 9660 tcttccgctt cctcgctcac tgactcgctg cgctcggtcg ttcggctgcg gcgagcggta 9720 tcagctcact caaaggcggt aatacggtta tccacagaat caggggataa cgcaggaaag 9780 aacatgtgag caaaaggcca gcaaaaggcc aggaaccgta aaaaggccgc gttgctggcg 9840 tttttccata ggctccgccc ccctgacgag catcacaaaa atcgacgctc aagtcagagg 9900 tggcgaaacc cgacaggact ataaagatac caggcgtttc cccctggaag ctccctcgtg 9960 cgctctcctg ttccgaccct gccgcttacc ggatacctgt ccgcctttct cccttcggga 10020 agcgtggcgc tttctcatag ctcacgctgt aggtatctca gttcggtgta ggtcgttcgc 10080 tccaagctgg gctgtgtgca cgaacccccc gttcagcccg accgctgcgc cttatccggt 10140 aactatcgtc ttgagtccaa cccggtaaga cacgacttat cgccactggc agcagccact 10200 ggtaacagga ttagcagagc gaggtatgta ggcggtgcta cagagttctt gaagtggtgg 10260 cctaactacg gctacactag aaggacagta tttggtatct gcgctctgct gaagccagtt 10320 accttcggaa aaagagttgg tagctcttga tccggcaaac aaaccaccgc tggtagcggt 10380 ggtttttttg tttgcaagca gcagattacg cgcagaaaaa aaggatctca agaagatcct 10440 ttgatctttt ctacggggtc tgacgctcag tggaacgaaa actcacgtta agggattttg 10500 gtcatgagat tatcaaaaag gatcttcacc tagatccttt taaattaaaa atgaagtttt 10560 aaatcaatct aaagtatata tgagtaaact tggtctgaca gttaccaatg cttaatcagt 10620 gaggcaccta tctcagcgat ctgtctattt cgttcatcca tagttgcctg actccccgtc 10680 gtgtagataa ctacgatacg ggagggctta ccatctggcc ccagtgctgc aatgataccg 10740 cgagacccac gctcaccggc tccagattta tcagcaataa accagccagc cggaagggcc 10800 gagcgcagaa gtggtcctgc aactttatcc gcctccatcc agtctattaa ttgttgccgg 10860 gaagctagag taagtagttc gccagttaat agtttgcgca acgttgttgc cattgctaca 10920 ggcatcgtgg tgtcacgctc gtcgtttggt atggcttcat tcagctccgg ttcccaacga 10980 tcaaggcgag ttacatgatc ccccatgttg tgcaaaaaag cggttagctc cttcggtcct 11040 ccgatcgttg tcagaagtaa gttggccgca gtgttatcac tcatggttat ggcagcactg 11100 cataattctc ttactgtcat gccatccgta agatgctttt ctgtgactgg tgagtactca 11160 accaagtcat tctgagaata gtgtatgcgg cgaccgagtt gctcttgccc ggcgtcaata 11220 cgggataata ccgcgccaca tagcagaact ttaaaagtgc tcatcattgg aaaacgttct 11280 tcggggcgaa aactctcaag gatcttaccg ctgttgagat ccagttcgat gtaacccact 11340 cgtgcaccca actgatcttc agcatctttt actttcacca gcgtttctgg gtgagcaaaa 11400 acaggaaggc aaaatgccgc aaaaaaggga ataagggcga cacggaaatg ttgaatactc 11460 atactcttcc tttttcaata ttattgaagc atttatcagg gttattgtct catgagcgga 11520 tacatatttg aatgtattta gaaaaataaa caaatagggg ttccgcgcac atttccccga 11580 aaagtgccac 11590 101 11593 DNA ARTIFICIAL SEQUENCE Synthetic 101 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgcga actcgatatt 1800 ttacacgact ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg aggggatcgc 3000 tctagagcga tccgggatct cgggaaaagc gttggtgacc aaaggtgcct tttatcatca 3060 ctttaaaaat aaaaaacaat tactcagtgc ctgttataag cagcaattaa ttatgattga 3120 tgcctacatc acaacaaaaa ctgatttaac aaatggttgg tctgccttag aaagtatatt 3180 tgaacattat cttgattata ttattgataa taataaaaac cttatcccta tccaagaagt 3240 gatgcctatc attggttgga atgaacttga aaaaaattag ccttgaatac attactggta 3300 aggtaaacgc cattgtcagc aaattgatcc aagagaacca acttaaagct ttcctgacgg 3360 aatgttaatt ctcgttgacc ctgagcactg atgaatcccc taatgatttt ggtaaaaatc 3420 attaagttaa ggtggataca catcttgtca tatgatcccg gtaatgtgag ttagctcact 3480 cattaggcac cccaggcttt acactttatg cttccggctc gtatgttgtg tggaattgtg 3540 agcggataac aatttcacac aggaaacagc tatgaccatg attacgccaa gcgcgcaatt 3600 aaccctcact aaagggaaca aaagctggag ctccaccgcg gtggcggccg ctctagaact 3660 agtggatccc ccgggctgca ggaattcgat atcaagctta tcgataccgc tgacctcgag 3720 catcagattg gctattggcc attgcatacg ttgtatccat atcataatat gtacatttat 3780 attggctcat gtccaacatt accgccatgt tgacattgat tattgactag ttattaatag 3840 taatcaatta cggggtcatt agttcatagc ccatatatgg agttccgcgt tacataactt 3900 acggtaaatg gcccgcctgg ctgaccgccc aacgaccccc gcccattgac gtcaataatg 3960 acgtatgttc ccatagtaac gccaataggg actttccatt gacgtcaatg ggtggagtat 4020 ttacggtaaa ctgcccactt ggcagtacat caagtgtatc atatgtcaag tacgccccct 4080 attgacgtca atgacggtaa atggcccgcc tggcattatg cccagtacat gaccttatgg 4140 gactttccta cttggcagta catctacgta ttagtcatcg ctattaccat ggtgatgcgg 4200 ttttggcagt acatcaatgg gcgtggatag cggtttgact cacggggatt tccaagtctt 4260 caccccattg acgtcaatgg gagtttgttt tggcaccaaa atcaacggga ctttccaaaa 4320 tgtcgtaaca actccgcccc attgacgcaa atgggcggta ggcgtgtacg gtgggaggtc 4380 tatataagca gagctcgttt agtgaaccgt cagatcgcct ggagacgcca tccacgctgt 4440 tttgacctcc atagaagaca ccgggaccga tccagcctcc gcggccggga acggtgcatt 4500 ggaacgcgga ttccccgtgc caagagtgac gtaagtaccg cctatagact ctataggcac 4560 acccctttgg ctcttatgca tgctatactg tttttggctt ggggcctata cacccccgct 4620 tccttatgct ataggtgatg gtatagctta gcctataggt gtgggttatt gaccattatt 4680 gaccactccc ctattggtga cgatactttc cattactaat ccataacatg gctctttgcc 4740 acaactatct ctattggcta tatgccaata ctctgtcctt cagagactga cacggactct 4800 gtatttttac aggatggggt cccatttatt atttacaaat tcacatatac aacaacgccg 4860 tcccccgtgc ccgcagtttt tattaaacat agcgtgggat ctccacgcga atctcgggta 4920 cgtgttccgg acatgggctc ttctccggta gcggcggagc ttccacatcc gagccctggt 4980 cccatgcctc cagcggctca tggtcgctcg gcagctcctt gctcctaaca gtggaggcca 5040 gacttaggca cagcacaatg cccaccacca ccagtgtgcc gcacaaggcc gtggcggtag 5100 ggtatgtgtc tgaaaatgag cgtggagatt gggctcgcac ggctgacgca gatggaagac 5160 ttaaggcagc ggcagaagaa gatgcaggca gctgagttgt tgtattctga taagagtcag 5220 aggtaactcc cgttgcggtg ctgttaacgg tggagggcag tgtagtctga gcagtactcg 5280 ttgctgccgc gcgcgccacc agacataata gctgacagac taacagactg ttcctttcca 5340 tgggtctttt ctgcagtcac cgtcggatca atcattcatc tcgtgacttc ttcgtgtgtg 5400 gtgtttacct atatatctaa atttaatatt tcgtttatta aaatttaata tatttcgacg 5460 atgaatttct caaggatatt tttcttcgtg ttcgctttgg ttctggcttt gtcaacagtt 5520 tcggctgcgc cagagccgaa aggtacccag gtgcagctgc aggagtcggg gggaggcttg 5580 gtaaagccgg gggggtccct tagagtctcc tgtgcagcct ctggattcac tttcagaaac 5640 gcctggatga gctgggtccg ccaggctcca gggaaggggc tggagtgggt cggccgtatt 5700 aaaagcaaaa ttgatggtgg gacaacagac tatgctgcac ccgtgaaagg cagattcacc 5760 atctcaagag atgattcaaa aaacacgtta tatctgcaaa tgaatagcct gaaagccgag 5820 gacacagccg tatattactg taccacgggg attatgataa catttggggg agttatccct 5880 cccccgaatt ggggccaggg aaccctggtc accgtctcct cagcctccac caagggccca 5940 tcggtcttcc ccctggcacc ctcctccaag agcacctctg ggggcacagc ggccctgggc 6000 tgcctggtca aggactactt ccccgaaccg gtgacggtgt cgtggaactc aggcgccctg 6060 accagcggcg tgcacacctt tccggctgtc ctacagtcct caggactcta cttccttagc 6120 aacgtggtga ccgtgccctc cagcagcttg ggcacccaga cctacatctg caacgtgaat 6180 cacaagccca gcaacaccaa ggtggacaag aaagttgagc ccaaatcttg tgacaaaact 6240 cacacatgcc caccgtgccc agcacctgaa ctcctggggg gaccgtcagt cttcctcttc 6300 cccccaaaac ccaaggacac cctcatgatc tcccggaccc ctgaggtcac atgcgtggtg 6360 gtggacgtga gccacgaaga ccctgaggtc aagttcaact ggtacgtgga cggcgtggag 6420 gtgcataatg ccaagacaaa gccgcgggag gagcagtaca acagcacgta ccgtgtggtc 6480 agcgtcctca ccgtcctgca ccaggactgg ctgaatggca aggagtacaa gtgcaaggtc 6540 tccaacaaag ccctcccagc ccccatcgag aaaaccatct ccaaagccaa agggcagccc 6600 cgagaaccac aggtgtacac cctgccccca tcccgggatg agctgaccaa gaaccaggtc 6660 agcctgacct gcctggtcaa aggcttctat cccagcgaca tcgccgtgga gtgggagagc 6720 aatgggcagc cggagaacaa ctacaagacc acgcctcccg tgctggactc cgacggctcc 6780 ttcttcctct acagcaagct caccgtggac aagagcaggt ggcagcaggg gaacgtcttc 6840 tcatgctccg tgatgcatga ggctctgcac aaccactaca cgcagaagag cctctccctg 6900 tctccgggta aagcgccaga gccgaaaaag ctttcctatg agctgacaca gccaccctcg 6960 gtgtcagtgt ccccaggaca aacggccagg atcacctgct ctggagatgc attgccagaa 7020 aaatatgttt attggtacca gcagaagtca ggccaggccc ctgtggtggt catctatgag 7080 gacagcaaac gaccctccgg gatccctgag agattctctg gctccagctc agggacaatg 7140 gccaccttga ctatcagtgg ggcccaggtg gaagatgaag gtgactacta ctgttactca 7200 actgacagca gtggttatca tagggaggtg ttcagcggag ggaccaagct gaccgtccta 7260 ggtcagccca aggctgcccc ctcggtcact ctgttcccac cctcctctga ggagcttcaa 7320 gccaacaagg ccacactggt gtgtctcata agtgactcct acccgggagc cgtgacagtg 7380 gcctggaagg cagatagcag ccccgtcaag gcgggagtgg agaccaccac accctccaaa 7440 caaagcaaca acaagtacgc ggccagcagc tacctgagcc tgacgcttga gcagtggaag 7500 tcccacaaaa gctacagctg ccaggtcacg catgaaggga gcaccgtgga gaagacagtg 7560 gcccctgcag aatgttcacc gcggagggag ggaagggccc tttttgaagg gggaggaaac 7620 ttcgcgccat gactcctctc gtgccccccg cacggaacac tgatgtgcag agggccctct 7680 gccattgctg cttcctctgc ccttcctcgt cactctgaat gtggcttctt tgctactgcc 7740 acagcaagaa ataaaatctc aacatctaaa tgggtttcct gagatttttc aagagtcgtt 7800 aagcacattc cttccccagc accccttgct gcaggccagt gccaggcacc aacttggcta 7860 ctgctgccca tgagagaaat ccagttcaat attttccaaa gcaaaatgga ttacatatgc 7920 cctagatcct gattaacagg tgttttgtat tatctgtgct ttcgcttcac ccacattatc 7980 ccattgcctc ccctcgaggg ggggcccggt acccaattcg ccctatagtg agtcgtatta 8040 cgcgcgctca ctggccgtcg ttttacaacg tcgtgactgg gaaaaccctg gcgttaccca 8100 acttaatcgc cttgcagcac atcccccttt cgccagctgg cgtaatagcg aagaggcccg 8160 caccgatcgc ccttcccaac agttgcgcag cctgaatggc gaatggaaat tgtaagcgtt 8220 aatattttgt taaaattcgc gttaaatttt tgttaaatca gctcattttt taaccaatag 8280 gccgaaatcg gcaaaatccc ttataaatca aaagaataga ccgagatagg gttgagtgtt 8340 gttccagttt ggaacaagag tccactatta aagaacgtgg actccaacgt caaagggcga 8400 aaaaccgtct atcagggcga tggcccacta ctccgggatc atatgacaag atgtgtatcc 8460 accttaactt aatgattttt accaaaatca ttaggggatt catcagtgct cagggtcaac 8520 gagaattaac attccgtcag gaaagcttat gatgatgatg tgcttaaaaa cttactcaat 8580 ggctggttat gcatatcgca atacatgcga aaaacctaaa agagcttgcc gataaaaaag 8640 gccaatttat tgctatttac cgcggctttt tattgagctt gaaagataaa taaaatagat 8700 aggttttatt tgaagctaaa tcttctttat cgtaaaaaat gccctcttgg gttatcaaga 8760 gggtcattat atttcgcgga ataacatcat ttggtgacga aataactaag cacttgtctc 8820 ctgtttactc ccctgagctt gaggggttaa catgaaggtc atcgatagca ggataataat 8880 acagtaaaac gctaaaccaa taatccaaat ccagccatcc caaattggta gtgaatgatt 8940 ataaataaca gcaaacagta atgggccaat aacaccggtt gcattggtaa ggctcaccaa 9000 taatccctgt aaagcacctt gctgatgact ctttgtttgg atagacatca ctccctgtaa 9060 tgcaggtaaa gcgatcccac caccagccaa taaaattaaa acagggaaaa ctaaccaacc 9120 ttcagatata aacgctaaaa aggcaaatgc actactatct gcaataaatc cgagcagtac 9180 tgccgttttt tcgcccattt agtggctatt cttcctgcca caaaggcttg gaatactgag 9240 tgtaaaagac caagacccgt aatgaaaagc caaccatcat gctattcatc atcacgattt 9300 ctgtaatagc accacaccgt gctggattgg ctatcaatgc gctgaaataa taatcaacaa 9360 atggcatcgt taaataagtg atgtataccg atcagctttt gttcccttta gtgagggtta 9420 attgcgcgct tggcgtaatc atggtcatag ctgtttcctg tgtgaaattg ttatccgctc 9480 acaattccac acaacatacg agccggaagc ataaagtgta aagcctgggg tgcctaatga 9540 gtgagctaac tcacattaat tgcgttgcgc tcactgcccg ctttccagtc gggaaacctg 9600 tcgtgccagc tgcattaatg aatcggccaa cgcgcgggga gaggcggttt gcgtattggg 9660 cgctcttccg cttcctcgct cactgactcg ctgcgctcgg tcgttcggct gcggcgagcg 9720 gtatcagctc actcaaaggc ggtaatacgg ttatccacag aatcagggga taacgcagga 9780 aagaacatgt gagcaaaagg ccagcaaaag gccaggaacc gtaaaaaggc cgcgttgctg 9840 gcgtttttcc ataggctccg cccccctgac gagcatcaca aaaatcgacg ctcaagtcag 9900 aggtggcgaa acccgacagg actataaaga taccaggcgt ttccccctgg aagctccctc 9960 gtgcgctctc ctgttccgac cctgccgctt accggatacc tgtccgcctt tctcccttcg 10020 ggaagcgtgg cgctttctca tagctcacgc tgtaggtatc tcagttcggt gtaggtcgtt 10080 cgctccaagc tgggctgtgt gcacgaaccc cccgttcagc ccgaccgctg cgccttatcc 10140 ggtaactatc gtcttgagtc caacccggta agacacgact tatcgccact ggcagcagcc 10200 actggtaaca ggattagcag agcgaggtat gtaggcggtg ctacagagtt cttgaagtgg 10260 tggcctaact acggctacac tagaaggaca gtatttggta tctgcgctct gctgaagcca 10320 gttaccttcg gaaaaagagt tggtagctct tgatccggca aacaaaccac cgctggtagc 10380 ggtggttttt ttgtttgcaa gcagcagatt acgcgcagaa aaaaaggatc tcaagaagat 10440 cctttgatct tttctacggg gtctgacgct cagtggaacg aaaactcacg ttaagggatt 10500 ttggtcatga gattatcaaa aaggatcttc acctagatcc ttttaaatta aaaatgaagt 10560 tttaaatcaa tctaaagtat atatgagtaa acttggtctg acagttacca atgcttaatc 10620 agtgaggcac ctatctcagc gatctgtcta tttcgttcat ccatagttgc ctgactcccc 10680 gtcgtgtaga taactacgat acgggagggc ttaccatctg gccccagtgc tgcaatgata 10740 ccgcgagacc cacgctcacc ggctccagat ttatcagcaa taaaccagcc agccggaagg 10800 gccgagcgca gaagtggtcc tgcaacttta tccgcctcca tccagtctat taattgttgc 10860 cgggaagcta gagtaagtag ttcgccagtt aatagtttgc gcaacgttgt tgccattgct 10920 acaggcatcg tggtgtcacg ctcgtcgttt ggtatggctt cattcagctc cggttcccaa 10980 cgatcaaggc gagttacatg atcccccatg ttgtgcaaaa aagcggttag ctccttcggt 11040 cctccgatcg ttgtcagaag taagttggcc gcagtgttat cactcatggt tatggcagca 11100 ctgcataatt ctcttactgt catgccatcc gtaagatgct tttctgtgac tggtgagtac 11160 tcaaccaagt cattctgaga atagtgtatg cggcgaccga gttgctcttg cccggcgtca 11220 atacgggata ataccgcgcc acatagcaga actttaaaag tgctcatcat tggaaaacgt 11280 tcttcggggc gaaaactctc aaggatctta ccgctgttga gatccagttc gatgtaaccc 11340 actcgtgcac ccaactgatc ttcagcatct tttactttca ccagcgtttc tgggtgagca 11400 aaaacaggaa ggcaaaatgc cgcaaaaaag ggaataaggg cgacacggaa atgttgaata 11460 ctcatactct tcctttttca atattattga agcatttatc agggttattg tctcatgagc 11520 ggatacatat ttgaatgtat ttagaaaaat aaacaaatag gggttccgcg cacatttccc 11580 cgaaaagtgc cac 11593 102 12339 DNA ARTIFICIAL SEQUENCE Synthetic 102 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgtga acttgatatt 1800 ttacatgatt ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg ataatgatcc 3000 agatcacttc tggctaataa aagatcagag ctctagagat ctgtgtgttg gttttttgtg 3060 gatctgctgt gccttctagt tgccagccat ctgttgtttg cccctccccc gtgccttcct 3120 tgaccctgga aggtgccact cccactgtcc tttcctaata aaatgaggaa attgcatcgc 3180 attgtctgag taggtgtcat tctattctgg ggggtggggt ggggcagcac agcaaggggg 3240 aggattggga agacaatagc aggcatgctg gggatgcggt gggctctatg ggtacctctc 3300 tctctctctc tctctctctc tctctctctc tctctcggta cctctctctc tctctctctc 3360 tctctctctc tctctctctc tcggtaccag gtgctgaaga attgacccgg tgaccaaagg 3420 tgccttttat catcacttta aaaataaaaa acaattactc agtgcctgtt ataagcagca 3480 attaattatg attgatgcct acatcacaac aaaaactgat ttaacaaatg gttggtctgc 3540 cttagaaagt atatttgaac attatcttga ttatattatt gataataata aaaaccttat 3600 ccctatccaa gaagtgatgc ctatcattgg ttggaatgaa cttgaaaaaa attagccttg 3660 aatacattac tggtaaggta aacgccattg tcagcaaatt gatccaagag aaccaactta 3720 aagctttcct gacggaatgt taattctcgt tgaccctgag cactgatgaa tcccctaatg 3780 attttggtaa aaatcattaa gttaaggtgg atacacatct tgtcatatga tcccggtaat 3840 gtgagttagc tcactcatta ggcaccccag gctttacact ttatgcttcc ggctcgtatg 3900 ttgtgtggaa ttgtgagcgg ataacaattt cacacaggaa acagctatga ccatgattac 3960 gccaagcgcg caattaaccc tcactaaagg gaacaaaagc tggagctcca ccgcggtggc 4020 ggccgctcta gaactagtgg atcccccggg ctgcaggaat tcgatatcaa gcttatcgat 4080 accgctgacc tcgagctgca gaaaaatgcc aggtggacta tgaactcaca tccaaaggag 4140 cttgacctga tacctgattt tcttcaaaca ggggaaacaa cacaatccca caaaacagct 4200 cagagagaaa ccatcactga tggctacagc accaaggtat gcaatggcaa tccattcgac 4260 attcatctgt gacctgagca aaatgatttc tctctccatg aatggttgct tctttccctc 4320 atgaaaaggc aatttccaca ctcacaatat gcgacaaaga caaacagaga acaattaatg 4380 tgctccttcc taatgtcaaa attgtagtgg caaagaggag aacaaaatct caagttctga 4440 gtaggtttta gtgattggat aagaggcttt gacctgtgag ctcacctgga cttcatatcc 4500 ttttggataa aaagtgcttt tataactttc aggtctccga gtctttattc atgagactgt 4560 tggtttaggg acagacccac aatgaaatgc ctggcatagg aaagggcagc agagccttag 4620 ctgacctttt cttgggacaa gcattgtcaa acaatgtgtg acaaaactat ttgtactgct 4680 ttgcacagct gtgctgggca gggcgatcca ttgccaccta tcccaggtaa ccttccaact 4740 gcaagaagat tgttgcttac tctctctaga aagcttctgc agactgacat gcatttcata 4800 ggtagagata acatttactg ggaagcacat ctatcatcac aaaaagcagg caagattttc 4860 agactttctt agtggctgaa atagaagcaa aagacgtaat taaaaacaaa atgaaacaaa 4920 aaaaatcagt tgatacctgt ggtgtagaca tccagcaaaa aaatattatt tgcactacca 4980 tcttgtctta agtcctcaga cttagcaagg agaatgtaga tttccacagt atatatgttt 5040 tcacaaaagg aaggagagaa acaaaagaaa atggcactga ctaaacttca gctagtggta 5100 taggaaagta attctgctta acagagattg cagtgatctc tatgtatgtc ctgaagaatt 5160 atgttgtact tttttccccc atttttaaat caaacagtgc tttacagagg tcagaatggt 5220 ttctttactg tttgtcaatt ctattatttc aatacagaac aatagcttct ataactgaaa 5280 tatatttgct attgtatatt atgattgtcc ctcgaaccat gaacactcct ccagctgaat 5340 ttcacaattc ctctgtcatc tgccaggcca ttaagttatt catggaagat ctttgaggaa 5400 cactgcaagt tcatatcata aacacatttg aaattgagta ttggtttgca ttgtatggag 5460 ctatgttttg ctgtatcctc agaaaaaaag tttgttataa agcattcaca cccataaaaa 5520 gatagattta aatattccag ctataggaaa gaaagtgcgt ctgctcttca ctctagtctc 5580 agttggctcc ttcacatgca tgcttcttta tttctcctat tttgtcaaga aaataatagg 5640 tcacgtcttg ttctcactta tgtcctgcct agcatggctc agatgcacgt tgtagataca 5700 agaaggatca aatgaaacag acttctggtc tgttacctac aaccatagta ataagcacac 5760 taactaataa ttgctaatta tgttttccat ctctaaggtt cccatatttt tctgttttct 5820 taaagatccc attatctggt tgtaactgaa gctcaatgga acatgagcaa tatttcccag 5880 tcttctctcc catccaacag tcctgatgga ttagcagaac aggcagaaaa cacattgtta 5940 cccagaatta aaaactaata tttgctctcc attcaatcca aaatggacct attgaaacta 6000 aaatctaacc caatcccatt aaatgatttc tatggtgtca aaggtcaaac ttctgaaggg 6060 aacctgtggg tgggtcacaa ttcaggctat atattcccca gggctcagcc agtggatcaa 6120 tcattcatct cgtgacttct tcgtgtgtgg tgtttaccta tatatctaaa tttaatattt 6180 cgtttattaa aatttaatat atttcgacga tgaatttctc aaggatattt ttcttcgtgt 6240 tcgctttggt tctggctttg tcaacagttt cggctgcgcc agagccgaaa ggtacccagg 6300 tgcagctgca ggagtcgggg ggaggcttgg taaagccggg ggggtccctt agagtctcct 6360 gtgcagcctc tggattcact ttcagaaacg cctggatgag ctgggtccgc caggctccag 6420 ggaaggggct ggagtgggtc ggccgtatta aaagcaaaat tgatggtggg acaacagact 6480 atgctgcacc cgtgaaaggc agattcacca tctcaagaga tgattcaaaa aacacgttat 6540 atctgcaaat gaatagcctg aaagccgagg acacagccgt atattactgt accacgggga 6600 ttatgataac atttggggga gttatccctc ccccgaattg gggccaggga accctggtca 6660 ccgtctcctc agcctccacc aagggcccat cggtcttccc cctggcaccc tcctccaaga 6720 gcacctctgg gggcacagcg gccctgggct gcctggtcaa ggactacttc cccgaaccgg 6780 tgacggtgtc gtggaactca ggcgccctga ccagcggcgt gcacaccttt ccggctgtcc 6840 tacagtcctc aggactctac ttccttagca acgtggtgac cgtgccctcc agcagcttgg 6900 gcacccagac ctacatctgc aacgtgaatc acaagcccag caacaccaag gtggacaaga 6960 aagttgagcc caaatcttgt gacaaaactc acacatgccc accgtgccca gcacctgaac 7020 tcctgggggg accgtcagtc ttcctcttcc ccccaaaacc caaggacacc ctcatgatct 7080 cccggacccc tgaggtcaca tgcgtggtgg tggacgtgag ccacgaagac cctgaggtca 7140 agttcaactg gtacgtggac ggcgtggagg tgcataatgc caagacaaag ccgcgggagg 7200 agcagtacaa cagcacgtac cgtgtggtca gcgtcctcac cgtcctgcac caggactggc 7260 tgaatggcaa ggagtacaag tgcaaggtct ccaacaaagc cctcccagcc cccatcgaga 7320 aaaccatctc caaagccaaa gggcagcccc gagaaccaca ggtgtacacc ctgcccccat 7380 cccgggatga gctgaccaag aaccaggtca gcctgacctg cctggtcaaa ggcttctatc 7440 ccagcgacat cgccgtggag tgggagagca atgggcagcc ggagaacaac tacaagacca 7500 cgcctcccgt gctggactcc gacggctcct tcttcctcta cagcaagctc accgtggaca 7560 agagcaggtg gcagcagggg aacgtcttct catgctccgt gatgcatgag gctctgcaca 7620 accactacac gcagaagagc ctctccctgt ctccgggtaa agcgccagag ccgaagcttt 7680 cctatgagct gacacagcca ccctcggtgt cagtgtcccc aggacaaacg gccaggatca 7740 cctgctctgg agatgcattg ccagaaaaat atgtttattg gtaccagcag aagtcaggcc 7800 aggcccctgt ggtggtcatc tatgaggaca gcaaacgacc ctccgggatc cctgagagat 7860 tctctggctc cagctcaggg acaatggcca ccttgactat cagtggggcc caggtggaag 7920 atgaaggtga ctactactgt tactcaactg acagcagtgg ttatcatagg gaggtgttca 7980 gcggagggac caagctgacc gtcctaggtc agcccaaggc tgccccctcg gtcactctgt 8040 tcccaccctc ctctgaggag cttcaagcca acaaggccac actggtgtgt ctcataagtg 8100 actcctaccc gggagccgtg acagtggcct ggaaggcaga tagcagcccc gtcaaggcgg 8160 gagtggagac caccacaccc tccaaacaaa gcaacaacaa gtacgcggcc agcagctacc 8220 tgagcctgac gcttgagcag tggaagtccc acaaaagcta cagctgccag gtcacgcatg 8280 aagggagcac cgtggagaag acagtggccc ctgcagaatg ttcaccgcgg agggagggaa 8340 gggccctttt tgaaggggga ggaaacttcg cgccatgact cctctcgtgc cccccgcacg 8400 gaacactgat gtgcagaggg ccctctgcca ttgctgcttc ctctgccctt cctcgtcact 8460 ctgaatgtgg cttctttgct actgccacag caagaaataa aatctcaaca tctaaatggg 8520 tttcctgaga tttttcaaga gtcgttaagc acattccttc cccagcaccc cttgctgcag 8580 gccagtgcca ggcaccaact tggctactgc tgcccatgag agaaatccag ttcaatattt 8640 tccaaagcaa aatggattac atatgcccta gatcctgatt aacaggtgtt ttgtattatc 8700 tgtgctttcg cttcacccac attatcccat tgcctcccct cgaggggggg cccggtaccc 8760 aattcgccct atagtgagtc gtattacgcg cgctcactgg ccgtcgtttt acaacgtcgt 8820 gactgggaaa accctggcgt tacccaactt aatcgccttg cagcacatcc ccctttcgcc 8880 agctggcgta atagcgaaga ggcccgcacc gatcgccctt cccaacagtt gcgcagcctg 8940 aatggcgaat ggaaattgta agcgttaata ttttgttaaa attcgcgtta aatttttgtt 9000 aaatcagctc attttttaac caataggccg aaatcggcaa aatcccttat aaatcaaaag 9060 aatagaccga gatagggttg agtgttgttc cagtttggaa caagagtcca ctattaaaga 9120 acgtggactc caacgtcaaa gggcgaaaaa ccgtctatca gggcgatggc ccactactcc 9180 gggatcatat gacaagatgt gtatccacct taacttaatg atttttacca aaatcattag 9240 gggattcatc agtgctcagg gtcaacgaga attaacattc cgtcaggaaa gcttatgatg 9300 atgatgtgct taaaaactta ctcaatggct ggttatgcat atcgcaatac atgcgaaaaa 9360 cctaaaagag cttgccgata aaaaaggcca atttattgct atttaccgcg gctttttatt 9420 gagcttgaaa gataaataaa atagataggt tttatttgaa gctaaatctt ctttatcgta 9480 aaaaatgccc tcttgggtta tcaagagggt cattatattt cgcggaataa catcatttgg 9540 tgacgaaata actaagcact tgtctcctgt ttactcccct gagcttgagg ggttaacatg 9600 aaggtcatcg atagcaggat aataatacag taaaacgcta aaccaataat ccaaatccag 9660 ccatcccaaa ttggtagtga atgattataa ataacagcaa acagtaatgg gccaataaca 9720 ccggttgcat tggtaaggct caccaataat ccctgtaaag caccttgctg atgactcttt 9780 gtttggatag acatcactcc ctgtaatgca ggtaaagcga tcccaccacc agccaataaa 9840 attaaaacag ggaaaactaa ccaaccttca gatataaacg ctaaaaaggc aaatgcacta 9900 ctatctgcaa taaatccgag cagtactgcc gttttttcgc ccatttagtg gctattcttc 9960 ctgccacaaa ggcttggaat actgagtgta aaagaccaag acccgtaatg aaaagccaac 10020 catcatgcta ttcatcatca cgatttctgt aatagcacca caccgtgctg gattggctat 10080 caatgcgctg aaataataat caacaaatgg catcgttaaa taagtgatgt ataccgatca 10140 gcttttgttc cctttagtga gggttaattg cgcgcttggc gtaatcatgg tcatagctgt 10200 ttcctgtgtg aaattgttat ccgctcacaa ttccacacaa catacgagcc ggaagcataa 10260 agtgtaaagc ctggggtgcc taatgagtga gctaactcac attaattgcg ttgcgctcac 10320 tgcccgcttt ccagtcggga aacctgtcgt gccagctgca ttaatgaatc ggccaacgcg 10380 cggggagagg cggtttgcgt attgggcgct cttccgcttc ctcgctcact gactcgctgc 10440 gctcggtcgt tcggctgcgg cgagcggtat cagctcactc aaaggcggta atacggttat 10500 ccacagaatc aggggataac gcaggaaaga acatgtgagc aaaaggccag caaaaggcca 10560 ggaaccgtaa aaaggccgcg ttgctggcgt ttttccatag gctccgcccc cctgacgagc 10620 atcacaaaaa tcgacgctca agtcagaggt ggcgaaaccc gacaggacta taaagatacc 10680 aggcgtttcc ccctggaagc tccctcgtgc gctctcctgt tccgaccctg ccgcttaccg 10740 gatacctgtc cgcctttctc ccttcgggaa gcgtggcgct ttctcatagc tcacgctgta 10800 ggtatctcag ttcggtgtag gtcgttcgct ccaagctggg ctgtgtgcac gaaccccccg 10860 ttcagcccga ccgctgcgcc ttatccggta actatcgtct tgagtccaac ccggtaagac 10920 acgacttatc gccactggca gcagccactg gtaacaggat tagcagagcg aggtatgtag 10980 gcggtgctac agagttcttg aagtggtggc ctaactacgg ctacactaga aggacagtat 11040 ttggtatctg cgctctgctg aagccagtta ccttcggaaa aagagttggt agctcttgat 11100 ccggcaaaca aaccaccgct ggtagcggtg gtttttttgt ttgcaagcag cagattacgc 11160 gcagaaaaaa aggatctcaa gaagatcctt tgatcttttc tacggggtct gacgctcagt 11220 ggaacgaaaa ctcacgttaa gggattttgg tcatgagatt atcaaaaagg atcttcacct 11280 agatcctttt aaattaaaaa tgaagtttta aatcaatcta aagtatatat gagtaaactt 11340 ggtctgacag ttaccaatgc ttaatcagtg aggcacctat ctcagcgatc tgtctatttc 11400 gttcatccat agttgcctga ctccccgtcg tgtagataac tacgatacgg gagggcttac 11460 catctggccc cagtgctgca atgataccgc gagacccacg ctcaccggct ccagatttat 11520 cagcaataaa ccagccagcc ggaagggccg agcgcagaag tggtcctgca actttatccg 11580 cctccatcca gtctattaat tgttgccggg aagctagagt aagtagttcg ccagttaata 11640 gtttgcgcaa cgttgttgcc attgctacag gcatcgtggt gtcacgctcg tcgtttggta 11700 tggcttcatt cagctccggt tcccaacgat caaggcgagt tacatgatcc cccatgttgt 11760 gcaaaaaagc ggttagctcc ttcggtcctc cgatcgttgt cagaagtaag ttggccgcag 11820 tgttatcact catggttatg gcagcactgc ataattctct tactgtcatg ccatccgtaa 11880 gatgcttttc tgtgactggt gagtactcaa ccaagtcatt ctgagaatag tgtatgcggc 11940 gaccgagttg ctcttgcccg gcgtcaatac gggataatac cgcgccacat agcagaactt 12000 taaaagtgct catcattgga aaacgttctt cggggcgaaa actctcaagg atcttaccgc 12060 tgttgagatc cagttcgatg taacccactc gtgcacccaa ctgatcttca gcatctttta 12120 ctttcaccag cgtttctggg tgagcaaaaa caggaaggca aaatgccgca aaaaagggaa 12180 taagggcgac acggaaatgt tgaatactca tactcttcct ttttcaatat tattgaagca 12240 tttatcaggg ttattgtctc atgagcggat acatatttga atgtatttag aaaaataaac 12300 aaataggggt tccgcgcaca tttccccgaa aagtgccac 12339 103 12342 DNA ARTIFICIAL SEQUENCE Synthetic 103 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgtga acttgatatt 1800 ttacatgatt ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg ataatgatcc 3000 agatcacttc tggctaataa aagatcagag ctctagagat ctgtgtgttg gttttttgtg 3060 gatctgctgt gccttctagt tgccagccat ctgttgtttg cccctccccc gtgccttcct 3120 tgaccctgga aggtgccact cccactgtcc tttcctaata aaatgaggaa attgcatcgc 3180 attgtctgag taggtgtcat tctattctgg ggggtggggt ggggcagcac agcaaggggg 3240 aggattggga agacaatagc aggcatgctg gggatgcggt gggctctatg ggtacctctc 3300 tctctctctc tctctctctc tctctctctc tctctcggta cctctctctc tctctctctc 3360 tctctctctc tctctctctc tcggtaccag gtgctgaaga attgacccgg tgaccaaagg 3420 tgccttttat catcacttta aaaataaaaa acaattactc agtgcctgtt ataagcagca 3480 attaattatg attgatgcct acatcacaac aaaaactgat ttaacaaatg gttggtctgc 3540 cttagaaagt atatttgaac attatcttga ttatattatt gataataata aaaaccttat 3600 ccctatccaa gaagtgatgc ctatcattgg ttggaatgaa cttgaaaaaa attagccttg 3660 aatacattac tggtaaggta aacgccattg tcagcaaatt gatccaagag aaccaactta 3720 aagctttcct gacggaatgt taattctcgt tgaccctgag cactgatgaa tcccctaatg 3780 attttggtaa aaatcattaa gttaaggtgg atacacatct tgtcatatga tcccggtaat 3840 gtgagttagc tcactcatta ggcaccccag gctttacact ttatgcttcc ggctcgtatg 3900 ttgtgtggaa ttgtgagcgg ataacaattt cacacaggaa acagctatga ccatgattac 3960 gccaagcgcg caattaaccc tcactaaagg gaacaaaagc tggagctcca ccgcggtggc 4020 ggccgctcta gaactagtgg atcccccggg ctgcaggaat tcgatatcaa gcttatcgat 4080 accgctgacc tcgagctgca gaaaaatgcc aggtggacta tgaactcaca tccaaaggag 4140 cttgacctga tacctgattt tcttcaaaca ggggaaacaa cacaatccca caaaacagct 4200 cagagagaaa ccatcactga tggctacagc accaaggtat gcaatggcaa tccattcgac 4260 attcatctgt gacctgagca aaatgatttc tctctccatg aatggttgct tctttccctc 4320 atgaaaaggc aatttccaca ctcacaatat gcgacaaaga caaacagaga acaattaatg 4380 tgctccttcc taatgtcaaa attgtagtgg caaagaggag aacaaaatct caagttctga 4440 gtaggtttta gtgattggat aagaggcttt gacctgtgag ctcacctgga cttcatatcc 4500 ttttggataa aaagtgcttt tataactttc aggtctccga gtctttattc atgagactgt 4560 tggtttaggg acagacccac aatgaaatgc ctggcatagg aaagggcagc agagccttag 4620 ctgacctttt cttgggacaa gcattgtcaa acaatgtgtg acaaaactat ttgtactgct 4680 ttgcacagct gtgctgggca gggcgatcca ttgccaccta tcccaggtaa ccttccaact 4740 gcaagaagat tgttgcttac tctctctaga aagcttctgc agactgacat gcatttcata 4800 ggtagagata acatttactg ggaagcacat ctatcatcac aaaaagcagg caagattttc 4860 agactttctt agtggctgaa atagaagcaa aagacgtaat taaaaacaaa atgaaacaaa 4920 aaaaatcagt tgatacctgt ggtgtagaca tccagcaaaa aaatattatt tgcactacca 4980 tcttgtctta agtcctcaga cttagcaagg agaatgtaga tttccacagt atatatgttt 5040 tcacaaaagg aaggagagaa acaaaagaaa atggcactga ctaaacttca gctagtggta 5100 taggaaagta attctgctta acagagattg cagtgatctc tatgtatgtc ctgaagaatt 5160 atgttgtact tttttccccc atttttaaat caaacagtgc tttacagagg tcagaatggt 5220 ttctttactg tttgtcaatt ctattatttc aatacagaac aatagcttct ataactgaaa 5280 tatatttgct attgtatatt atgattgtcc ctcgaaccat gaacactcct ccagctgaat 5340 ttcacaattc ctctgtcatc tgccaggcca ttaagttatt catggaagat ctttgaggaa 5400 cactgcaagt tcatatcata aacacatttg aaattgagta ttggtttgca ttgtatggag 5460 ctatgttttg ctgtatcctc agaaaaaaag tttgttataa agcattcaca cccataaaaa 5520 gatagattta aatattccag ctataggaaa gaaagtgcgt ctgctcttca ctctagtctc 5580 agttggctcc ttcacatgca tgcttcttta tttctcctat tttgtcaaga aaataatagg 5640 tcacgtcttg ttctcactta tgtcctgcct agcatggctc agatgcacgt tgtagataca 5700 agaaggatca aatgaaacag acttctggtc tgttacctac aaccatagta ataagcacac 5760 taactaataa ttgctaatta tgttttccat ctctaaggtt cccatatttt tctgttttct 5820 taaagatccc attatctggt tgtaactgaa gctcaatgga acatgagcaa tatttcccag 5880 tcttctctcc catccaacag tcctgatgga ttagcagaac aggcagaaaa cacattgtta 5940 cccagaatta aaaactaata tttgctctcc attcaatcca aaatggacct attgaaacta 6000 aaatctaacc caatcccatt aaatgatttc tatggtgtca aaggtcaaac ttctgaaggg 6060 aacctgtggg tgggtcacaa ttcaggctat atattcccca gggctcagcc agtggatcaa 6120 tcattcatct cgtgacttct tcgtgtgtgg tgtttaccta tatatctaaa tttaatattt 6180 cgtttattaa aatttaatat atttcgacga tgaatttctc aaggatattt ttcttcgtgt 6240 tcgctttggt tctggctttg tcaacagttt cggctgcgcc agagccgaaa ggtacccagg 6300 tgcagctgca ggagtcgggg ggaggcttgg taaagccggg ggggtccctt agagtctcct 6360 gtgcagcctc tggattcact ttcagaaacg cctggatgag ctgggtccgc caggctccag 6420 ggaaggggct ggagtgggtc ggccgtatta aaagcaaaat tgatggtggg acaacagact 6480 atgctgcacc cgtgaaaggc agattcacca tctcaagaga tgattcaaaa aacacgttat 6540 atctgcaaat gaatagcctg aaagccgagg acacagccgt atattactgt accacgggga 6600 ttatgataac atttggggga gttatccctc ccccgaattg gggccaggga accctggtca 6660 ccgtctcctc agcctccacc aagggcccat cggtcttccc cctggcaccc tcctccaaga 6720 gcacctctgg gggcacagcg gccctgggct gcctggtcaa ggactacttc cccgaaccgg 6780 tgacggtgtc gtggaactca ggcgccctga ccagcggcgt gcacaccttt ccggctgtcc 6840 tacagtcctc aggactctac ttccttagca acgtggtgac cgtgccctcc agcagcttgg 6900 gcacccagac ctacatctgc aacgtgaatc acaagcccag caacaccaag gtggacaaga 6960 aagttgagcc caaatcttgt gacaaaactc acacatgccc accgtgccca gcacctgaac 7020 tcctgggggg accgtcagtc ttcctcttcc ccccaaaacc caaggacacc ctcatgatct 7080 cccggacccc tgaggtcaca tgcgtggtgg tggacgtgag ccacgaagac cctgaggtca 7140 agttcaactg gtacgtggac ggcgtggagg tgcataatgc caagacaaag ccgcgggagg 7200 agcagtacaa cagcacgtac cgtgtggtca gcgtcctcac cgtcctgcac caggactggc 7260 tgaatggcaa ggagtacaag tgcaaggtct ccaacaaagc cctcccagcc cccatcgaga 7320 aaaccatctc caaagccaaa gggcagcccc gagaaccaca ggtgtacacc ctgcccccat 7380 cccgggatga gctgaccaag aaccaggtca gcctgacctg cctggtcaaa ggcttctatc 7440 ccagcgacat cgccgtggag tgggagagca atgggcagcc ggagaacaac tacaagacca 7500 cgcctcccgt gctggactcc gacggctcct tcttcctcta cagcaagctc accgtggaca 7560 agagcaggtg gcagcagggg aacgtcttct catgctccgt gatgcatgag gctctgcaca 7620 accactacac gcagaagagc ctctccctgt ctccgggtaa agcgccagag ccgaaaaagc 7680 tttcctatga gctgacacag ccaccctcgg tgtcagtgtc cccaggacaa acggccagga 7740 tcacctgctc tggagatgca ttgccagaaa aatatgttta ttggtaccag cagaagtcag 7800 gccaggcccc tgtggtggtc atctatgagg acagcaaacg accctccggg atccctgaga 7860 gattctctgg ctccagctca gggacaatgg ccaccttgac tatcagtggg gcccaggtgg 7920 aagatgaagg tgactactac tgttactcaa ctgacagcag tggttatcat agggaggtgt 7980 tcagcggagg gaccaagctg accgtcctag gtcagcccaa ggctgccccc tcggtcactc 8040 tgttcccacc ctcctctgag gagcttcaag ccaacaaggc cacactggtg tgtctcataa 8100 gtgactccta cccgggagcc gtgacagtgg cctggaaggc agatagcagc cccgtcaagg 8160 cgggagtgga gaccaccaca ccctccaaac aaagcaacaa caagtacgcg gccagcagct 8220 acctgagcct gacgcttgag cagtggaagt cccacaaaag ctacagctgc caggtcacgc 8280 atgaagggag caccgtggag aagacagtgg cccctgcaga atgttcaccg cggagggagg 8340 gaagggccct ttttgaaggg ggaggaaact tcgcgccatg actcctctcg tgccccccgc 8400 acggaacact gatgtgcaga gggccctctg ccattgctgc ttcctctgcc cttcctcgtc 8460 actctgaatg tggcttcttt gctactgcca cagcaagaaa taaaatctca acatctaaat 8520 gggtttcctg agatttttca agagtcgtta agcacattcc ttccccagca ccccttgctg 8580 caggccagtg ccaggcacca acttggctac tgctgcccat gagagaaatc cagttcaata 8640 ttttccaaag caaaatggat tacatatgcc ctagatcctg attaacaggt gttttgtatt 8700 atctgtgctt tcgcttcacc cacattatcc cattgcctcc cctcgagggg gggcccggta 8760 cccaattcgc cctatagtga gtcgtattac gcgcgctcac tggccgtcgt tttacaacgt 8820 cgtgactggg aaaaccctgg cgttacccaa cttaatcgcc ttgcagcaca tccccctttc 8880 gccagctggc gtaatagcga agaggcccgc accgatcgcc cttcccaaca gttgcgcagc 8940 ctgaatggcg aatggaaatt gtaagcgtta atattttgtt aaaattcgcg ttaaattttt 9000 gttaaatcag ctcatttttt aaccaatagg ccgaaatcgg caaaatccct tataaatcaa 9060 aagaatagac cgagataggg ttgagtgttg ttccagtttg gaacaagagt ccactattaa 9120 agaacgtgga ctccaacgtc aaagggcgaa aaaccgtcta tcagggcgat ggcccactac 9180 tccgggatca tatgacaaga tgtgtatcca ccttaactta atgattttta ccaaaatcat 9240 taggggattc atcagtgctc agggtcaacg agaattaaca ttccgtcagg aaagcttatg 9300 atgatgatgt gcttaaaaac ttactcaatg gctggttatg catatcgcaa tacatgcgaa 9360 aaacctaaaa gagcttgccg ataaaaaagg ccaatttatt gctatttacc gcggcttttt 9420 attgagcttg aaagataaat aaaatagata ggttttattt gaagctaaat cttctttatc 9480 gtaaaaaatg ccctcttggg ttatcaagag ggtcattata tttcgcggaa taacatcatt 9540 tggtgacgaa ataactaagc acttgtctcc tgtttactcc cctgagcttg aggggttaac 9600 atgaaggtca tcgatagcag gataataata cagtaaaacg ctaaaccaat aatccaaatc 9660 cagccatccc aaattggtag tgaatgatta taaataacag caaacagtaa tgggccaata 9720 acaccggttg cattggtaag gctcaccaat aatccctgta aagcaccttg ctgatgactc 9780 tttgtttgga tagacatcac tccctgtaat gcaggtaaag cgatcccacc accagccaat 9840 aaaattaaaa cagggaaaac taaccaacct tcagatataa acgctaaaaa ggcaaatgca 9900 ctactatctg caataaatcc gagcagtact gccgtttttt cgcccattta gtggctattc 9960 ttcctgccac aaaggcttgg aatactgagt gtaaaagacc aagacccgta atgaaaagcc 10020 aaccatcatg ctattcatca tcacgatttc tgtaatagca ccacaccgtg ctggattggc 10080 tatcaatgcg ctgaaataat aatcaacaaa tggcatcgtt aaataagtga tgtataccga 10140 tcagcttttg ttccctttag tgagggttaa ttgcgcgctt ggcgtaatca tggtcatagc 10200 tgtttcctgt gtgaaattgt tatccgctca caattccaca caacatacga gccggaagca 10260 taaagtgtaa agcctggggt gcctaatgag tgagctaact cacattaatt gcgttgcgct 10320 cactgcccgc tttccagtcg ggaaacctgt cgtgccagct gcattaatga atcggccaac 10380 gcgcggggag aggcggtttg cgtattgggc gctcttccgc ttcctcgctc actgactcgc 10440 tgcgctcggt cgttcggctg cggcgagcgg tatcagctca ctcaaaggcg gtaatacggt 10500 tatccacaga atcaggggat aacgcaggaa agaacatgtg agcaaaaggc cagcaaaagg 10560 ccaggaaccg taaaaaggcc gcgttgctgg cgtttttcca taggctccgc ccccctgacg 10620 agcatcacaa aaatcgacgc tcaagtcaga ggtggcgaaa cccgacagga ctataaagat 10680 accaggcgtt tccccctgga agctccctcg tgcgctctcc tgttccgacc ctgccgctta 10740 ccggatacct gtccgccttt ctcccttcgg gaagcgtggc gctttctcat agctcacgct 10800 gtaggtatct cagttcggtg taggtcgttc gctccaagct gggctgtgtg cacgaacccc 10860 ccgttcagcc cgaccgctgc gccttatccg gtaactatcg tcttgagtcc aacccggtaa 10920 gacacgactt atcgccactg gcagcagcca ctggtaacag gattagcaga gcgaggtatg 10980 taggcggtgc tacagagttc ttgaagtggt ggcctaacta cggctacact agaaggacag 11040 tatttggtat ctgcgctctg ctgaagccag ttaccttcgg aaaaagagtt ggtagctctt 11100 gatccggcaa acaaaccacc gctggtagcg gtggtttttt tgtttgcaag cagcagatta 11160 cgcgcagaaa aaaaggatct caagaagatc ctttgatctt ttctacgggg tctgacgctc 11220 agtggaacga aaactcacgt taagggattt tggtcatgag attatcaaaa aggatcttca 11280 cctagatcct tttaaattaa aaatgaagtt ttaaatcaat ctaaagtata tatgagtaaa 11340 cttggtctga cagttaccaa tgcttaatca gtgaggcacc tatctcagcg atctgtctat 11400 ttcgttcatc catagttgcc tgactccccg tcgtgtagat aactacgata cgggagggct 11460 taccatctgg ccccagtgct gcaatgatac cgcgagaccc acgctcaccg gctccagatt 11520 tatcagcaat aaaccagcca gccggaaggg ccgagcgcag aagtggtcct gcaactttat 11580 ccgcctccat ccagtctatt aattgttgcc gggaagctag agtaagtagt tcgccagtta 11640 atagtttgcg caacgttgtt gccattgcta caggcatcgt ggtgtcacgc tcgtcgtttg 11700 gtatggcttc attcagctcc ggttcccaac gatcaaggcg agttacatga tcccccatgt 11760 tgtgcaaaaa agcggttagc tccttcggtc ctccgatcgt tgtcagaagt aagttggccg 11820 cagtgttatc actcatggtt atggcagcac tgcataattc tcttactgtc atgccatccg 11880 taagatgctt ttctgtgact ggtgagtact caaccaagtc attctgagaa tagtgtatgc 11940 ggcgaccgag ttgctcttgc ccggcgtcaa tacgggataa taccgcgcca catagcagaa 12000 ctttaaaagt gctcatcatt ggaaaacgtt cttcggggcg aaaactctca aggatcttac 12060 cgctgttgag atccagttcg atgtaaccca ctcgtgcacc caactgatct tcagcatctt 12120 ttactttcac cagcgtttct gggtgagcaa aaacaggaag gcaaaatgcc gcaaaaaagg 12180 gaataagggc gacacggaaa tgttgaatac tcatactctt cctttttcaa tattattgaa 12240 gcatttatca gggttattgt ctcatgagcg gatacatatt tgaatgtatt tagaaaaata 12300 aacaaatagg ggttccgcgc acatttcccc gaaaagtgcc ac 12342 104 11970 DNA ARTIFICIAL SEQUENCE Synthetic 104 ctgacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 60 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 120 ccacgttcgc cggcatcaga ttggctattg gccattgcat acgttgtatc catatcataa 180 tatgtacatt tatattggct catgtccaac attaccgcca tgttgacatt gattattgac 240 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 300 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 360 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 420 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 480 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 540 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 600 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 660 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 720 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 780 acggtgggag gtctatataa gcagagctcg tttagtgaac cgtcagatcg cctggagacg 840 ccatccacgc tgttttgacc tccatagaag acaccgggac cgatccagcc tccgcggccg 900 ggaacggtgc attggaacgc ggattccccg tgccaagagt gacgtaagta ccgcctatag 960 actctatagg cacacccctt tggctcttat gcatgctata ctgtttttgg cttggggcct 1020 atacaccccc gcttccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 1080 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1140 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1200 tgacacggac tctgtatttt tacaggatgg ggtcccattt attatttaca aattcacata 1260 tacaacaacg ccgtcccccg tgcccgcagt ttttattaaa catagcgtgg gatctccacg 1320 cgaatctcgg gtacgtgttc cggacatggg ctcttctccg gtagcggcgg agcttccaca 1380 tccgagccct ggtcccatgc ctccagcggc tcatggtcgc tcggcagctc cttgctccta 1440 acagtggagg ccagacttag gcacagcaca atgcccacca ccaccagtgt gccgcacaag 1500 gccgtggcgg tagggtatgt gtctgaaaat gagcgtggag attgggctcg cacggctgac 1560 gcagatggaa gacttaaggc agcggcagaa gaagatgcag gcagctgagt tgttgtattc 1620 tgataagagt cagaggtaac tcccgttgcg gtgctgttaa cggtggaggg cagtgtagtc 1680 tgagcagtac tcgttgctgc cgcgcgcgcc accagacata atagctgaca gactaacaga 1740 ctgttccttt ccatgggtct tttctgcagt caccgtcgga ccatgtgtga acttgatatt 1800 ttacatgatt ctctttacca attctgcccc gaattacact taaaacgact caacagctta 1860 acgttggctt gccacgcatt acttgactgt aaaactctca ctcttaccga acttggccgt 1920 aacctgccaa ccaaagcgag aacaaaacat aacatcaaac gaatcgaccg attgttaggt 1980 aatcgtcacc tccacaaaga gcgactcgct gtataccgtt ggcatgctag ctttatctgt 2040 tcgggcaata cgatgcccat tgtacttgtt gactggtctg atattcgtga gcaaaaacga 2100 cttatggtat tgcgagcttc agtcgcacta cacggtcgtt ctgttactct ttatgagaaa 2160 gcgttcccgc tttcagagca atgttcaaag aaagctcatg accaatttct agccgacctt 2220 gcgagcattc taccgagtaa caccacaccg ctcattgtca gtgatgctgg ctttaaagtg 2280 ccatggtata aatccgttga gaagctgggt tggtactggt taagtcgagt aagaggaaaa 2340 gtacaatatg cagacctagg agcggaaaac tggaaaccta tcagcaactt acatgatatg 2400 tcatctagtc actcaaagac tttaggctat aagaggctga ctaaaagcaa tccaatctca 2460 tgccaaattc tattgtataa atctcgctct aaaggccgaa aaaatcagcg ctcgacacgg 2520 actcattgtc accacccgtc acctaaaatc tactcagcgt cggcaaagga gccatgggtt 2580 ctagcaacta acttacctgt tgaaattcga acacccaaac aacttgttaa tatctattcg 2640 aagcgaatgc agattgaaga aaccttccga gacttgaaaa gtcctgccta cggactaggc 2700 ctacgccata gccgaacgag cagctcagag cgttttgata tcatgctgct aatcgccctg 2760 atgcttcaac taacatgttg gcttgcgggc gttcatgctc agaaacaagg ttgggacaag 2820 cacttccagg ctaacacagt cagaaatcga aacgtactct caacagttcg cttaggcatg 2880 gaagttttgc ggcattctgg ctacacaata acaagggaag acttactcgt ggctgcaacc 2940 ctactagctc aaaatttatt cacacatggt tacgctttgg ggaaattatg ataatgatcc 3000 agatcacttc tggctaataa aagatcagag ctctagagat ctgtgtgttg gttttttgtg 3060 gatctgctgt gccttctagt tgccagccat ctgttgtttg cccctccccc gtgccttcct 3120 tgaccctgga aggtgccact cccactgtcc tttcctaata aaatgaggaa attgcatcgc 3180 attgtctgag taggtgtcat tctattctgg ggggtggggt ggggcagcac agcaaggggg 3240 aggattggga agacaatagc aggcatgctg gggatgcggt gggctctatg ggtacctctc 3300 tctctctctc tctctctctc tctctctctc tctctcggta cctctctctc tctctctctc 3360 tctctctctc tctctctctc tcggtaccag gtgctgaaga attgacccgg tgaccaaagg 3420 tgccttttat catcacttta aaaataaaaa acaattactc agtgcctgtt ataagcagca 3480 attaattatg attgatgcct acatcacaac aaaaactgat ttaacaaatg gttggtctgc 3540 cttagaaagt atatttgaac attatcttga ttatattatt gataataata aaaaccttat 3600 ccctatccaa gaagtgatgc ctatcattgg ttggaatgaa cttgaaaaaa attagccttg 3660 aatacattac tggtaaggta aacgccattg tcagcaaatt gatccaagag aaccaactta 3720 aagctttcct gacggaatgt taattctcgt tgaccctgag cactgatgaa tcccctaatg 3780 attttggtaa aaatcattaa gttaaggtgg atacacatct tgtcatatga tcccggtaat 3840 gtgagttagc tcactcatta ggcaccccag gctttacact ttatgcttcc ggctcgtatg 3900 ttgtgtggaa ttgtgagcgg ataacaattt cacacaggaa acagctatga ccatgattac 3960 gccaagcgcg caattaaccc tcactaaagg gaacaaaagc tggagctcca ccgcggtggc 4020 ggccgctcta gaactagtgg atcccccggg ctgcaggaat tcgatatcaa gcttatcgat 4080 accgctgacc tcgagcatca gattggctat tggccattgc atacgttgta tccatatcat 4140 aatatgtaca tttatattgg ctcatgtcca acattaccgc catgttgaca ttgattattg 4200 actagttatt aatagtaatc aattacgggg tcattagttc atagcccata tatggagttc 4260 cgcgttacat aacttacggt aaatggcccg cctggctgac cgcccaacga cccccgccca 4320 ttgacgtcaa taatgacgta tgttcccata gtaacgccaa tagggacttt ccattgacgt 4380 caatgggtgg agtatttacg gtaaactgcc cacttggcag tacatcaagt gtatcatatg 4440 tcaagtacgc cccctattga cgtcaatgac ggtaaatggc ccgcctggca ttatgcccag 4500 tacatgacct tatgggactt tcctacttgg cagtacatct acgtattagt catcgctatt 4560 accatggtga tgcggttttg gcagtacatc aatgggcgtg gatagcggtt tgactcacgg 4620 ggatttccaa gtcttcaccc cattgacgtc aatgggagtt tgttttggca ccaaaatcaa 4680 cgggactttc caaaatgtcg taacaactcc gccccattga cgcaaatggg cggtaggcgt 4740 gtacggtggg aggtctatat aagcagagct cgtttagtga accgtcagat cgcctggaga 4800 cgccatccac gctgttttga cctccataga agacaccggg accgatccag cctccgcggc 4860 cgggaacggt gcattggaac gcggattccc cgtgccaaga gtgacgtaag taccgcctat 4920 agactctata ggcacacccc tttggctctt atgcatgcta tactgttttt ggcttggggc 4980 ctatacaccc ccgcttcctt atgctatagg tgatggtata gcttagccta taggtgtggg 5040 ttattgacca ttattgacca ctcccctatt ggtgacgata ctttccatta ctaatccata 5100 acatggctct ttgccacaac tatctctatt ggctatatgc caatactctg tccttcagag 5160 actgacacgg actctgtatt tttacaggat ggggtcccat ttattattta caaattcaca 5220 tatacaacaa cgccgtcccc cgtgcccgca gtttttatta aacatagcgt gggatctcca 5280 cgcgaatctc gggtacgtgt tccggacatg ggctcttctc cggtagcggc ggagcttcca 5340 catccgagcc ctggtcccat gcctccagcg gctcatggtc gctcggcagc tccttgctcc 5400 taacagtgga ggccagactt aggcacagca caatgcccac caccaccagt gtgccgcaca 5460 aggccgtggc ggtagggtat gtgtctgaaa atgagcgtgg agattgggct cgcacggctg 5520 acgcagatgg aagacttaag gcagcggcag aagaagatgc aggcagctga gttgttgtat 5580 tctgataaga gtcagaggta actcccgttg cggtgctgtt aacggtggag ggcagtgtag 5640 tctgagcagt actcgttgct gccgcgcgcg ccaccagaca taatagctga cagactaaca 5700 gactgttcct ttccatgggt cttttctgca gtcaccgtcg gatcaatcat tcatctcgtg 5760 acttcttcgt gtgtggtgtt tacctatata tctaaattta atatttcgtt tattaaaatt 5820 taatatattt cgacgatgaa tttctcaagg atatttttct tcgtgttcgc tttggttctg 5880 gctttgtcaa cagtttcggc tgcgccagag ccgaaaggta cccaggtgca gctgcaggag 5940 tcggggggag gcttggtaaa gccggggggg tcccttagag tctcctgtgc agcctctgga 6000 ttcactttca gaaacgcctg gatgagctgg gtccgccagg ctccagggaa ggggctggag 6060 tgggtcggcc gtattaaaag caaaattgat ggtgggacaa cagactatgc tgcacccgtg 6120 aaaggcagat tcaccatctc aagagatgat tcaaaaaaca cgttatatct gcaaatgaat 6180 agcctgaaag ccgaggacac agccgtatat tactgtacca cggggattat gataacattt 6240 gggggagtta tccctccccc gaattggggc cagggaaccc tggtcaccgt ctcctcagcc 6300 tccaccaagg gcccatcggt cttccccctg gcaccctcct ccaagagcac ctctgggggc 6360 acagcggccc tgggctgcct ggtcaaggac tacttccccg aaccggtgac ggtgtcgtgg 6420 aactcaggcg ccctgaccag cggcgtgcac acctttccgg ctgtcctaca gtcctcagga 6480 ctctacttcc ttagcaacgt ggtgaccgtg ccctccagca gcttgggcac ccagacctac 6540 atctgcaacg tgaatcacaa gcccagcaac accaaggtgg acaagaaagt tgagcccaaa 6600 tcttgtgaca aaactcacac atgcccaccg tgcccagcac ctgaactcct ggggggaccg 6660 tcagtcttcc tcttcccccc aaaacccaag gacaccctca tgatctcccg gacccctgag 6720 gtcacatgcg tggtggtgga cgtgagccac gaagaccctg aggtcaagtt caactggtac 6780 gtggacggcg tggaggtgca taatgccaag acaaagccgc gggaggagca gtacaacagc 6840 acgtaccgtg tggtcagcgt cctcaccgtc ctgcaccagg actggctgaa tggcaaggag 6900 tacaagtgca aggtctccaa caaagccctc ccagccccca tcgagaaaac catctccaaa 6960 gccaaagggc agccccgaga accacaggtg tacaccctgc ccccatcccg ggatgagctg 7020 accaagaacc aggtcagcct gacctgcctg gtcaaaggct tctatcccag cgacatcgcc 7080 gtggagtggg agagcaatgg gcagccggag aacaactaca agaccacgcc tcccgtgctg 7140 gactccgacg gctccttctt cctctacagc aagctcaccg tggacaagag caggtggcag 7200 caggggaacg tcttctcatg ctccgtgatg catgaggctc tgcacaacca ctacacgcag 7260 aagagcctct ccctgtctcc gggtaaagcg ccagagccga agctttccta tgagctgaca 7320 cagccaccct cggtgtcagt gtccccagga caaacggcca ggatcacctg ctctggagat 7380 gcattgccag aaaaatatgt ttattggtac cagcagaagt caggccaggc ccctgtggtg 7440 gtcatctatg aggacagcaa acgaccctcc gggatccctg agagattctc tggctccagc 7500 tcagggacaa tggccacctt gactatcagt ggggcccagg tggaagatga aggtgactac 7560 tactgttact caactgacag cagtggttat catagggagg tgttcagcgg agggaccaag 7620 ctgaccgtcc taggtcagcc caaggctgcc ccctcggtca ctctgttccc accctcctct 7680 gaggagcttc aagccaacaa ggccacactg gtgtgtctca taagtgactc ctacccggga 7740 gccgtgacag tggcctggaa ggcagatagc agccccgtca aggcgggagt ggagaccacc 7800 acaccctcca aacaaagcaa caacaagtac gcggccagca gctacctgag cctgacgctt 7860 gagcagtgga agtcccacaa aagctacagc tgccaggtca cgcatgaagg gagcaccgtg 7920 gagaagacag tggcccctgc agaatgttca ccgcggaggg agggaagggc cctttttgaa 7980 gggggaggaa acttcgcgcc atgactcctc tcgtgccccc cgcacggaac actgatgtgc 8040 agagggccct ctgccattgc tgcttcctct gcccttcctc gtcactctga atgtggcttc 8100 tttgctactg ccacagcaag aaataaaatc tcaacatcta aatgggtttc ctgagatttt 8160 tcaagagtcg ttaagcacat tccttcccca gcaccccttg ctgcaggcca gtgccaggca 8220 ccaacttggc tactgctgcc catgagagaa atccagttca atattttcca aagcaaaatg 8280 gattacatat gccctagatc ctgattaaca ggtgttttgt attatctgtg ctttcgcttc 8340 acccacatta tcccattgcc tcccctcgac tcgagggggg gcccggtacc caattcgccc 8400 tatagtgagt cgtattacgc gcgctcactg gccgtcgttt tacaacgtcg tgactgggaa 8460 aaccctggcg ttacccaact taatcgcctt gcagcacatc cccctttcgc cagctggcgt 8520 aatagcgaag aggcccgcac cgatcgccct tcccaacagt tgcgcagcct gaatggcgaa 8580 tggaaattgt aagcgttaat attttgttaa aattcgcgtt aaatttttgt taaatcagct 8640 cattttttaa ccaataggcc gaaatcggca aaatccctta taaatcaaaa gaatagaccg 8700 agatagggtt gagtgttgtt ccagtttgga acaagagtcc actattaaag aacgtggact 8760 ccaacgtcaa agggcgaaaa accgtctatc agggcgatgg cccactactc cgggatcata 8820 tgacaagatg tgtatccacc ttaacttaat gatttttacc aaaatcatta ggggattcat 8880 cagtgctcag ggtcaacgag aattaacatt ccgtcaggaa agcttatgat gatgatgtgc 8940 ttaaaaactt actcaatggc tggttatgca tatcgcaata catgcgaaaa acctaaaaga 9000 gcttgccgat aaaaaaggcc aatttattgc tatttaccgc ggctttttat tgagcttgaa 9060 agataaataa aatagatagg ttttatttga agctaaatct tctttatcgt aaaaaatgcc 9120 ctcttgggtt atcaagaggg tcattatatt tcgcggaata acatcatttg gtgacgaaat 9180 aactaagcac ttgtctcctg tttactcccc tgagcttgag gggttaacat gaaggtcatc 9240 gatagcagga taataataca gtaaaacgct aaaccaataa tccaaatcca gccatcccaa 9300 attggtagtg aatgattata aataacagca aacagtaatg ggccaataac accggttgca 9360 ttggtaaggc tcaccaataa tccctgtaaa gcaccttgct gatgactctt tgtttggata 9420 gacatcactc cctgtaatgc aggtaaagcg atcccaccac cagccaataa aattaaaaca 9480 gggaaaacta accaaccttc agatataaac gctaaaaagg caaatgcact actatctgca 9540 ataaatccga gcagtactgc cgttttttcg cccatttagt ggctattctt cctgccacaa 9600 aggcttggaa tactgagtgt aaaagaccaa gacccgtaat gaaaagccaa ccatcatgct 9660 attcatcatc acgatttctg taatagcacc acaccgtgct ggattggcta tcaatgcgct 9720 gaaataataa tcaacaaatg gcatcgttaa ataagtgatg tataccgatc agcttttgtt 9780 ccctttagtg agggttaatt gcgcgcttgg cgtaatcatg gtcatagctg tttcctgtgt 9840 gaaattgtta tccgctcaca attccacaca acatacgagc cggaagcata aagtgtaaag 9900 cctggggtgc ctaatgagtg agctaactca cattaattgc gttgcgctca ctgcccgctt 9960 tccagtcggg aaacctgtcg tgccagctgc attaatgaat cggccaacgc gcggggagag 10020 gcggtttgcg tattgggcgc tcttccgctt cctcgctcac tgactcgctg cgctcggtcg 10080 ttcggctgcg gcgagcggta tcagctcact caaaggcggt aatacggtta tccacagaat 10140 caggggataa cgcaggaaag aacatgtgag caaaaggcca gcaaaaggcc aggaaccgta 10200 aaaaggccgc gttgctggcg tttttccata ggctccgccc ccctgacgag catcacaaaa 10260 atcgacgctc aagtcagagg tggcgaaacc cgacaggact ataaagatac caggcgtttc 10320 cccctggaag ctccctcgtg cgctctcctg ttccgaccct gccgcttacc ggatacctgt 10380 ccgcctttct cccttcggga agcgtggcgc tttctcatag ctcacgctgt aggtatctca 10440 gttcggtgta ggtcgttcgc tccaagctgg gctgtgtgca cgaacccccc gttcagcccg 10500 accgctgcgc cttatccggt aactatcgtc ttgagtccaa cccggtaaga cacgacttat 10560 cgccactggc agcagccact ggtaacagga ttagcagagc gaggtatgta ggcggtgcta 10620 cagagttctt gaagtggtgg cctaactacg gctacactag aaggacagta tttggtatct 10680 gcgctctgct gaagccagtt accttcggaa aaagagttgg tagctcttga tccggcaaac 10740 aaaccaccgc tggtagcggt ggtttttttg tttgcaagca gcagattacg cgcagaaaaa 10800 aaggatctca agaagatcct ttgatctttt ctacggggtc tgacgctcag tggaacgaaa 10860 actcacgtta agggattttg gtcatgagat tatcaaaaag gatcttcacc tagatccttt 10920 taaattaaaa atgaagtttt aaatcaatct aaagtatata tgagtaaact tggtctgaca 10980 gttaccaatg cttaatcagt gaggcaccta tctcagcgat ctgtctattt cgttcatcca 11040 tagttgcctg actccccgtc gtgtagataa ctacgatacg ggagggctta ccatctggcc 11100 ccagtgctgc aatgataccg cgagacccac gctcaccggc tccagattta tcagcaataa 11160 accagccagc cggaagggcc gagcgcagaa gtggtcctgc aactttatcc gcctccatcc 11220 agtctattaa ttgttgccgg gaagctagag taagtagttc gccagttaat agtttgcgca 11280 acgttgttgc cattgctaca ggcatcgtgg tgtcacgctc gtcgtttggt atggcttcat 11340 tcagctccgg ttcccaacga tcaaggcgag ttacatgatc ccccatgttg tgcaaaaaag 11400 cggttagctc cttcggtcct ccgatcgttg tcagaagtaa gttggccgca gtgttatcac 11460 tcatggttat ggcagcactg cataattctc ttactgtcat gccatccgta agatgctttt 11520 ctgtgactgg tgagtactca accaagtcat tctgagaata gtgtatgcgg cgaccgagtt 11580 gctcttgccc ggcgtcaata cgggataata ccgcgccaca tagcagaact ttaaaagtgc 11640 tcatcattgg aaaacgttct tcggggcgaa aactctcaag gatcttaccg ctgttgagat 11700 ccagttcgat gtaacccact cgtgcaccca actgatcttc agcatctttt actttcacca 11760 gcgtttctgg gtgagcaaaa acaggaaggc aaaatgccgc aaaaaaggga ataagggcga 11820 cacggaaatg ttgaatactc atactcttcc tttttcaata ttattgaagc atttatcagg 11880 gttattgtct catgagcgga tacatatttg aatgtattta gaaaaataaa caaatagggg 11940 ttccgcgcac atttccccga aaagtgccac 11970 

We claim:
 1. An isolated polynucleotide comprising two or more genes of interest and two or more pro nucleotide sequences, wherein each gene of interest is operably-linked to a pro nucleotide sequence and each of the two or more genes of interest may be the same or different.
 2. The polynucleotide of claim 1, wherein a most 5′ pro nucleotide sequence of the two or more pro nucleotide sequences is a part of a prepro nucleotide sequence.
 3. The polynucleotide of claim 2, wherein the prepro nucleotide sequence is a cecropin prepro nucleotide sequence.
 4. The polynucleotide of claim 2, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:3.
 5. The polynucleotide of claim 2, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:4.
 6. The polynucleotide of claim 1, wherein the two or more pro nucleotide sequences each comprise a cecropin pro nucleotide sequence.
 7. The polynucleotide of claim 1, wherein the two or more pro nucleotide sequences each comprise a sequence shown in SEQ ID NO:1.
 8. The polynucleotide of claim 1, wherein the two or more pro nucleotide sequences each comprise a sequence shown in SEQ ID NO:2.
 9. The polynucleotide of claim 1, wherein two genes of interest and two pro nucleotide sequences are arranged in the following order: a prepro nucleotide sequence, a first gene of interest, a pro nucleotide sequence, and a second gene of interest.
 10. The polynucleotide of claim 9, wherein the prepro nucleotide sequence is a cecropin prepro nucleotide sequence and the pro nucleotide sequence is a cecropin pro nucleotide sequence.
 11. The polynucleotide of claim 9, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:3 or SEQ ID NO:4 and the pro nucleotide sequence comprises a sequence shown in SEQ ID NO:1 or SEQ ID NO:2.
 12. The polynucleotide of claim 1, wherein a first gene of interest encodes for an antibody heavy chain and a second gene of interest encodes for an antibody light chain.
 13. A method of producing a multimeric protein in an individual comprising administering to the individual a polynucleotide comprising two or more genes of interest, wherein each gene of interest encodes a part of the multimeric protein, each gene of interest is operably-linked to a pro nucleotide sequence, and each of the two or more genes of interest may be the same or different.
 14. The method of claim 13, wherein the multimeric protein is an associated multimeric protein.
 15. The method of claim 13, wherein the multimeric protein is a multivalent multimeric protein.
 16. The method of claim 13, wherein the pro nucleotide sequence comprises a cecropin pro nucleotide sequence.
 17. The method of claim 13, wherein the pro nucleotide sequence comprises a sequence shown in SEQ ID NO:1.
 18. The method of claim 13, wherein the pro nucleotide sequence comprises a sequence shown in SEQ ID NO:2.
 19. The method of claim 13, wherein a most 5′ pro nucleotide sequence of the two or more pro sequences is a part of a prepro nucleotide sequence.
 20. The method of claim 19, wherein the prepro nucleotide sequence is a cecropin prepro nucleotide sequence.
 21. The method of claim 19, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:3.
 22. The method of claim 19, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:4.
 23. The method of claim 19, wherein the polynucleotide comprises two genes of interest and two pro nucleotide sequences arranged in the following order: a prepro nucleotide sequence, a first gene of interest, a pro nucleotide sequence, and a second gene of interest.
 24. The method of claim 13, wherein a first gene of interest encodes for an antibody heavy chain and a second gene of interest encodes for an antibody light chain.
 25. A method of producing a protein in an individual comprising administering to the individual a polynucleotide comprising a cecropin prepro nucleotide sequence operably-linked to one or more genes of interest that encode the protein.
 26. The method of claim 25, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:3.
 27. The method of claim 25, wherein the prepro nucleotide sequence comprises a sequence shown in SEQ ID NO:4.
 28. The method of claim 25, wherein a first gene of interest is an antibody heavy chain and a second gene of interest is an antibody light chain.
 29. The method of claim 25, wherein the protein is a multimeric protein and the cecropin prepro nucleotide sequence is operably-linked to two or more genes of interest, wherein each gene of interest encodes a part of the multimeric protein.
 30. The method of claim 29, wherein the multimeric protein is an associated multimeric protein.
 31. The method of claim 29, wherein the multimeric protein is a multivalent multimeric protein.
 32. A method of producing a multimeric protein in an individual comprising administering to the individual a polynucleotide comprising two or more genes of interest, wherein each gene of interest encodes a part of the multimeric protein and wherein each gene of interest is operably linked to a gene encoding for a cleavage site.
 33. The method of claim 32, wherein a transposon-based vector comprises the polynucleotide and further comprises a transposase gene operably linked to a first promoter and wherein; a) the first promoter comprises a modified Kozak sequence comprising ACCATG; b) the two or more genes of interest are each operably-linked to one or more additional promoters; and, c) the two or more genes of interest and their operably-linked promoters are flanked by transposase insertion sequences recognized by a transposase encoded by the transposase gene.
 34. The method of claim 32, wherein a transposon-based vector comprises the polynucleotide and further comprises a transposase gene operably linked to a first promoter and an avian optimized polyA sequence, and wherein; a) the two or more genes of interest are each operably-linked to one or more additional promoters; and, b) the two or more genes of interest and their operably-linked promoters are flanked by transposase insertion sequences recognized by a transposase encoded by the transposase gene.
 35. The method of claim 32, wherein the cleavage site is selected from a protease cleavage site, a photolabile cleavage site, a pH sensitive cleavage site, a chemical cleavage site and a self-splicing cleavage site.
 36. An animal comprising the isolated polynucleotide of claim
 1. 37. The animal of claim 36, wherein the animal is a bird.
 38. An egg produced by the animal of claim
 37. 39. The egg of claim 38, wherein the egg comprises a multimeric protein encoded by the isolated polynucleotide.
 40. The animal of claim 36, wherein the animal is a mammal.
 41. Milk produced by the mammal of claim
 40. 42. The milk of claim 41, wherein the milk comprises a multimeric protein encoded by the isolated polynucleotide.
 43. A method of producing a multimeric protein comprising: a) administering to an egg-laying animal a composition comprising the polynucleotide of claim 1; and, b) permitting the one or more genes of interest to be expressed into the multimeric protein.
 44. The method of claim 43, further comprising a) collecting an egg from the egg-laying animal; b) harvesting egg white comprising the multimeric protein; and, c) purifying the multimeric protein.
 45. The method of claim 43, wherein the egg-laying animal is a bird.
 46. A method of producing a multimeric protein comprising: a) administering to an intramammary duct system of a mammal a composition comprising the polynucleotide of claim 1, and, b) permitting the one or more genes of interest to be expressed into the multimeric protein.
 47. The method of claim 46, further comprising a) collecting milk from the mammal, wherein the milk comprises the multimeric protein; and b) purifying the multimeric protein. 